Canonical Allele Identifier: CA2620916395
Gene: MYL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.110911003G>A , CM000674.2:g.110911003G>A GRCh38
NC_000012.11:g.111348807G>A , CM000674.1:g.111348807G>A GRCh37
NC_000012.10:g.109833190G>A NCBI36
NG_007554.1:g.14575C>T , LRG_393:g.14575C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000228841.15:c.*74C>T MANE Select ENSP00000228841.8:n.*74C>T
ENST00000663220.1:c.*74C>T ENSP00000499568.1:n.*74C>T
ENST00000228841.12:c.*74C>T ENSP00000228841.7:n.*74C>T
ENST00000548438.1:c.*74C>T ENSP00000447154.1:n.*74C>T
NM_000432.3:c.*74C>T , LRG_393t1:c.*74C>T NP_000423.2:n.*74C>T
NM_000432.4:c.*74C>T MANE Select NP_000423.2:n.*74C>T