Canonical Allele Identifier: CA343774266
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173878926A>G (hg19) chr1:g.173909788A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909788A>G , CM000663.2:g.173909788A>G GRCh38
NC_000001.10:g.173878926A>G , CM000663.1:g.173878926A>G GRCh37
NC_000001.9:g.172145549A>G NCBI36
NG_012462.1:g.12591T>C , LRG_577:g.12591T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.917T>C MANE Select ENSP00000356671.3:p.Phe306Ser
ENST00000367698.3:c.917T>C ENSP00000356671.3:p.Phe306Ser
ENST00000487183.1:n.568T>C
ENST00000617423.4:c.559+2076T>C ENSP00000478688.1:n.559+2076T>C
NM_000488.3:c.917T>C , LRG_577t1:c.917T>C NP_000479.1:p.Phe306Ser
XM_005245198.2:c.773T>C XP_005245255.1:p.Phe258Ser
NM_001365052.1:c.773T>C NP_001351981.1:p.Phe258Ser
NM_000488.4:c.917T>C MANE Select NP_000479.1:p.Phe306Ser
NM_001365052.2:c.773T>C NP_001351981.1:p.Phe258Ser
NM_001386302.1:c.1040T>C NP_001373231.1:p.Phe347Ser
NM_001386303.1:c.998T>C NP_001373232.1:p.Phe333Ser
NM_001386304.1:c.896T>C NP_001373233.1:p.Phe299Ser
NM_001386305.1:c.860T>C NP_001373234.1:p.Phe287Ser
NM_001386306.1:c.701T>C NP_001373235.1:p.Phe234Ser
Search 100 bp 5'
Search 100 bp 3'