Canonical Allele Identifier: CA036291
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1585700
ClinVar RCV Id: RCV002095595
dbSNP Id: rs747292416

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23422160G>A , CM000676.2:g.23422160G>A GRCh38
NC_000014.8:g.23891369G>A , CM000676.1:g.23891369G>A GRCh37
NC_000014.7:g.22961209G>A NCBI36
NG_007884.1:g.18502C>T , LRG_384:g.18502C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3245+20C>T MANE Select ENSP00000347507.3:n.3245+20C>T
ENST00000355349.3:c.3245+20C>T ENSP00000347507.3:n.3245+20C>T
NM_000257.3:c.3245+20C>T NP_000248.2:n.3245+20C>T
XR_245686.3:n.3351+20C>T
XM_017021340.1:c.3245+20C>T XP_016876829.1:n.3245+20C>T
NM_000257.4:c.3245+20C>T MANE Select NP_000248.2:n.3245+20C>T