Canonical Allele Identifier: CA389040587
Gene: MYH7 HGNC NCBI

Linked Data

dbSNP Id: rs2138646975

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23417673G>A , CM000676.2:g.23417673G>A GRCh38
NC_000014.8:g.23886882G>A , CM000676.1:g.23886882G>A GRCh37
NC_000014.7:g.22956722G>A NCBI36
NG_007884.1:g.22989C>T , LRG_384:g.22989C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4183C>T MANE Select ENSP00000347507.3:p.Gln1395Ter
ENST00000355349.3:c.4183C>T ENSP00000347507.3:p.Gln1395Ter
NM_000257.3:c.4183C>T NP_000248.2:p.Gln1395Ter
XM_017021340.1:c.4183C>T XP_016876829.1:p.Gln1395Ter
NM_000257.4:c.4183C>T MANE Select NP_000248.2:p.Gln1395Ter