Canonical Allele Identifier: CA612937385
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1544860
ClinVar RCV Id: RCV002165357
dbSNP Id: rs1320579178

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23423538T>A , CM000676.2:g.23423538T>A GRCh38
NC_000014.8:g.23892747T>A , CM000676.1:g.23892747T>A GRCh37
NC_000014.7:g.22962587T>A NCBI36
NG_007884.1:g.17124A>T , LRG_384:g.17124A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3099+9A>T MANE Select ENSP00000347507.3:n.3099+9A>T
ENST00000355349.3:c.3099+9A>T ENSP00000347507.3:n.3099+9A>T
NM_000257.3:c.3099+9A>T NP_000248.2:n.3099+9A>T
XR_245686.3:n.3205+9A>T
XM_017021340.1:c.3099+9A>T XP_016876829.1:n.3099+9A>T
NM_000257.4:c.3099+9A>T MANE Select NP_000248.2:n.3099+9A>T