Canonical Allele Identifier: CA389052492
Gene: MYH7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431820A>T , CM000676.2:g.23431820A>T GRCh38
NC_000014.8:g.23901029A>T , CM000676.1:g.23901029A>T GRCh37
NC_000014.7:g.22970869A>T NCBI36
NG_007884.1:g.8842T>A , LRG_384:g.8842T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.580T>A MANE Select ENSP00000347507.3:p.Tyr194Asn
ENST00000355349.3:c.580T>A ENSP00000347507.3:p.Tyr194Asn
NM_000257.3:c.580T>A NP_000248.2:p.Tyr194Asn
XR_245686.3:n.686T>A
XM_017021340.1:c.580T>A XP_016876829.1:p.Tyr194Asn
NM_000257.4:c.580T>A MANE Select NP_000248.2:p.Tyr194Asn