Canonical Allele Identifier: CA612937502
Gene: MYH7 HGNC NCBI

Linked Data

dbSNP Id: rs1302410026

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23424184G>C , CM000676.2:g.23424184G>C GRCh38
NC_000014.8:g.23893393G>C , CM000676.1:g.23893393G>C GRCh37
NC_000014.7:g.22963233G>C NCBI36
NG_007884.1:g.16478C>G , LRG_384:g.16478C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.2680-35C>G MANE Select ENSP00000347507.3:n.2680-35C>G
ENST00000355349.3:c.2680-35C>G ENSP00000347507.3:n.2680-35C>G
NM_000257.3:c.2680-35C>G NP_000248.2:n.2680-35C>G
XR_245686.3:n.2786-35C>G
XM_017021340.1:c.2680-35C>G XP_016876829.1:n.2680-35C>G
NM_000257.4:c.2680-35C>G MANE Select NP_000248.2:n.2680-35C>G