Canonical Allele Identifier: CA027479
Gene: MYH7 HGNC NCBI

Linked Data

dbSNP Id: rs778313325

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23433628C>T , CM000676.2:g.23433628C>T GRCh38
NC_000014.8:g.23902837C>T , CM000676.1:g.23902837C>T GRCh37
NC_000014.7:g.22972677C>T NCBI36
NG_007884.1:g.7034G>A , LRG_384:g.7034G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000355349.4:c.105G>A MANE Select ENSP00000347507.3:p.Lys35=
ENST00000355349.3:c.105G>A ENSP00000347507.3:p.Lys35=
NM_000257.3:c.105G>A NP_000248.2:p.Lys35=
XR_245686.3:n.211G>A
XM_017021340.1:c.105G>A XP_016876829.1:p.Lys35=
NM_000257.4:c.105G>A MANE Select NP_000248.2:p.Lys35=