Canonical Allele Identifier: CA2573149858
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1614361
ClinVar RCV Id: RCV002075908
dbSNP Id: rs2138662822

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23423737A>C , CM000676.2:g.23423737A>C GRCh38
NC_000014.8:g.23892946A>C , CM000676.1:g.23892946A>C GRCh37
NC_000014.7:g.22962786A>C NCBI36
NG_007884.1:g.16925T>G , LRG_384:g.16925T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.2923-14T>G MANE Select ENSP00000347507.3:n.2923-14T>G
ENST00000355349.3:c.2923-14T>G ENSP00000347507.3:n.2923-14T>G
NM_000257.3:c.2923-14T>G NP_000248.2:n.2923-14T>G
XR_245686.3:n.3029-14T>G
XM_017021340.1:c.2923-14T>G XP_016876829.1:n.2923-14T>G
NM_000257.4:c.2923-14T>G MANE Select NP_000248.2:n.2923-14T>G