Canonical Allele Identifier: CA485767411
Gene: MYH7 HGNC NCBI

Linked Data

dbSNP Id: rs1892957282
MyVariant Identifiers: chr14:g.23901036G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431827G>A , CM000676.2:g.23431827G>A GRCh38
NC_000014.8:g.23901036G>A , CM000676.1:g.23901036G>A GRCh37
NC_000014.7:g.22970876G>A NCBI36
NG_007884.1:g.8835C>T , LRG_384:g.8835C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.573C>T MANE Select ENSP00000347507.3:p.Val191=
ENST00000355349.3:c.573C>T ENSP00000347507.3:p.Val191=
NM_000257.3:c.573C>T NP_000248.2:p.Val191=
XR_245686.3:n.679C>T
XM_017021340.1:c.573C>T XP_016876829.1:p.Val191=
NM_000257.4:c.573C>T MANE Select NP_000248.2:p.Val191=