Canonical Allele Identifier: CA047123
Gene: MYH7 HGNC NCBI

Linked Data

dbSNP Id: rs775357831

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431848C>T , CM000676.2:g.23431848C>T GRCh38
NC_000014.8:g.23901057C>T , CM000676.1:g.23901057C>T GRCh37
NC_000014.7:g.22970897C>T NCBI36
NG_007884.1:g.8814G>A , LRG_384:g.8814G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.552G>A MANE Select ENSP00000347507.3:p.Lys184=
ENST00000355349.3:c.552G>A ENSP00000347507.3:p.Lys184=
NM_000257.3:c.552G>A NP_000248.2:p.Lys184=
XR_245686.3:n.658G>A
XM_017021340.1:c.552G>A XP_016876829.1:p.Lys184=
NM_000257.4:c.552G>A MANE Select NP_000248.2:p.Lys184=