Canonical Allele Identifier: CA029331
Gene: MYH7 HGNC NCBI

Linked Data

dbSNP Id: rs771132107

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23433558C>A , CM000676.2:g.23433558C>A GRCh38
NC_000014.8:g.23902767C>A , CM000676.1:g.23902767C>A GRCh37
NC_000014.7:g.22972607C>A NCBI36
NG_007884.1:g.7104G>T , LRG_384:g.7104G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000355349.4:c.175G>T MANE Select ENSP00000347507.3:p.Val59Phe
ENST00000355349.3:c.175G>T ENSP00000347507.3:p.Val59Phe
NM_000257.3:c.175G>T NP_000248.2:p.Val59Phe
XR_245686.3:n.281G>T
XM_017021340.1:c.175G>T XP_016876829.1:p.Val59Phe
NM_000257.4:c.175G>T MANE Select NP_000248.2:p.Val59Phe