Canonical Allele Identifier: CA485617843
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 525110
ClinVar RCV Id: RCV000629135
dbSNP Id: rs763934978

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23417605G>A , CM000676.2:g.23417605G>A GRCh38
NC_000014.8:g.23886814G>A , CM000676.1:g.23886814G>A GRCh37
NC_000014.7:g.22956654G>A NCBI36
NG_007884.1:g.23057C>T , LRG_384:g.23057C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4251C>T MANE Select ENSP00000347507.3:p.Thr1417=
ENST00000355349.3:c.4251C>T ENSP00000347507.3:p.Thr1417=
NM_000257.3:c.4251C>T NP_000248.2:p.Thr1417=
XM_017021340.1:c.4251C>T XP_016876829.1:p.Thr1417=
NM_000257.4:c.4251C>T MANE Select NP_000248.2:p.Thr1417=