Canonical Allele Identifier: CA343774748
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173879047T>C (hg19) chr1:g.173909909T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909909T>C , CM000663.2:g.173909909T>C GRCh38
NC_000001.10:g.173879047T>C , CM000663.1:g.173879047T>C GRCh37
NC_000001.9:g.172145670T>C NCBI36
NG_012462.1:g.12470A>G , LRG_577:g.12470A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.796A>G MANE Select ENSP00000356671.3:p.Thr266Ala
ENST00000367698.3:c.796A>G ENSP00000356671.3:p.Thr266Ala
ENST00000487183.1:n.447A>G
ENST00000617423.4:c.559+1955A>G ENSP00000478688.1:n.559+1955A>G
NM_000488.3:c.796A>G , LRG_577t1:c.796A>G NP_000479.1:p.Thr266Ala
XM_005245198.2:c.652A>G XP_005245255.1:p.Thr218Ala
NM_001365052.1:c.652A>G NP_001351981.1:p.Thr218Ala
NM_000488.4:c.796A>G MANE Select NP_000479.1:p.Thr266Ala
NM_001365052.2:c.652A>G NP_001351981.1:p.Thr218Ala
NM_001386302.1:c.919A>G NP_001373231.1:p.Thr307Ala
NM_001386303.1:c.877A>G NP_001373232.1:p.Thr293Ala
NM_001386304.1:c.775A>G NP_001373233.1:p.Thr259Ala
NM_001386305.1:c.763-24A>G NP_001373234.1:n.763-24A>G
NM_001386306.1:c.580A>G NP_001373235.1:p.Thr194Ala
Search 100 bp 5'
Search 100 bp 3'