Canonical Allele Identifier: CA2063066137
Gene: MYL2 HGNC NCBI

Linked Data

dbSNP Id: rs1592798234

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.110910910A>G , CM000674.2:g.110910910A>G GRCh38
NC_000012.11:g.111348714A>G , CM000674.1:g.111348714A>G GRCh37
NC_000012.10:g.109833097A>G NCBI36
NG_007554.1:g.14668T>C , LRG_393:g.14668T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000228841.15:c.*167T>C MANE Select ENSP00000228841.8:n.*167T>C
ENST00000663220.1:c.*167T>C ENSP00000499568.1:n.*167T>C
ENST00000228841.12:c.*167T>C ENSP00000228841.7:n.*167T>C
NM_000432.3:c.*167T>C , LRG_393t1:c.*167T>C NP_000423.2:n.*167T>C
NM_000432.4:c.*167T>C MANE Select NP_000423.2:n.*167T>C