Canonical Allele Identifier: CA951809917
Gene: MYL2 HGNC NCBI

Linked Data

dbSNP Id: rs1014672113

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.110910906G>A , CM000674.2:g.110910906G>A GRCh38
NC_000012.11:g.111348710G>A , CM000674.1:g.111348710G>A GRCh37
NC_000012.10:g.109833093G>A NCBI36
NG_007554.1:g.14672C>T , LRG_393:g.14672C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000228841.15:c.*171C>T MANE Select ENSP00000228841.8:n.*171C>T
ENST00000663220.1:c.*171C>T ENSP00000499568.1:n.*171C>T
ENST00000228841.12:c.*171C>T ENSP00000228841.7:n.*171C>T
NM_000432.3:c.*171C>T , LRG_393t1:c.*171C>T NP_000423.2:n.*171C>T
NM_000432.4:c.*171C>T MANE Select NP_000423.2:n.*171C>T