Canonical Allele Identifier: CA485617774

Linked Data

ClinVar Variation Id: 2188244
ClinVar RCV Id: RCV002620085
dbSNP Id: rs1595075235
MyVariant Identifiers: chr14:g.23886754A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23417545A>C , CM000676.2:g.23417545A>C GRCh38
NC_000014.8:g.23886754A>C , CM000676.1:g.23886754A>C GRCh37
NC_000014.7:g.22956594A>C NCBI36
NG_007884.1:g.23117T>G , LRG_384:g.23117T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4311T>G (MYH7) MANE Select ENSP00000347507.3:p.Ala1437=
ENST00000355349.3:c.4311T>G (MYH7) ENSP00000347507.3:p.Ala1437=
NM_000257.3:c.4311T>G (MYH7) NP_000248.2:p.Ala1437=
NR_126491.1:n.826A>C (MHRT)
XM_017021340.1:c.4311T>G (MYH7) XP_016876829.1:p.Ala1437=
NM_000257.4:c.4311T>G (MYH7) MANE Select NP_000248.2:p.Ala1437=