Canonical Allele Identifier: CA257825944
Gene: MYH7 HGNC NCBI

Linked Data

dbSNP Id: rs113884995

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431593A>G , CM000676.2:g.23431593A>G GRCh38
NC_000014.8:g.23900802A>G , CM000676.1:g.23900802A>G GRCh37
NC_000014.7:g.22970642A>G NCBI36
NG_007884.1:g.9069T>C , LRG_384:g.9069T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.724T>C MANE Select ENSP00000347507.3:p.Ser242Pro
ENST00000355349.3:c.724T>C ENSP00000347507.3:p.Ser242Pro
NM_000257.3:c.724T>C NP_000248.2:p.Ser242Pro
XR_245686.3:n.830T>C
XM_017021340.1:c.724T>C XP_016876829.1:p.Ser242Pro
NM_000257.4:c.724T>C MANE Select NP_000248.2:p.Ser242Pro