Canonical Allele Identifier: CA389052442
Gene: MYH7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431796C>A , CM000676.2:g.23431796C>A GRCh38
NC_000014.8:g.23901005C>A , CM000676.1:g.23901005C>A GRCh37
NC_000014.7:g.22970845C>A NCBI36
NG_007884.1:g.8866G>T , LRG_384:g.8866G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.604G>T MANE Select ENSP00000347507.3:p.Gly202Trp
ENST00000355349.3:c.604G>T ENSP00000347507.3:p.Gly202Trp
NM_000257.3:c.604G>T NP_000248.2:p.Gly202Trp
XR_245686.3:n.710G>T
XM_017021340.1:c.604G>T XP_016876829.1:p.Gly202Trp
NM_000257.4:c.604G>T MANE Select NP_000248.2:p.Gly202Trp