Canonical Allele Identifier: CA961070264
Gene: MYH7 HGNC NCBI

Linked Data

dbSNP Id: rs1555338600
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431164C>A , CM000676.2:g.23431164C>A GRCh38
NC_000014.8:g.23900373C>A , CM000676.1:g.23900373C>A GRCh37
NC_000014.7:g.22970213C>A NCBI36
NG_007884.1:g.9498G>T , LRG_384:g.9498G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.797-165G>T MANE Select ENSP00000347507.3:n.797-165G>T
ENST00000355349.3:c.797-165G>T ENSP00000347507.3:n.797-165G>T
NM_000257.3:c.797-165G>T NP_000248.2:n.797-165G>T
XR_245686.3:n.903-165G>T
XM_017021340.1:c.797-165G>T XP_016876829.1:n.797-165G>T
NM_000257.4:c.797-165G>T MANE Select NP_000248.2:n.797-165G>T
Search 100 bp 5'
Search 100 bp 3'