Canonical Allele Identifier: CA2620916322
Gene: MYL2 HGNC NCBI

Linked Data

gnomAD v4: 12-110910918-C-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.110910918C>A , CM000674.2:g.110910918C>A GRCh38
NC_000012.11:g.111348722C>A , CM000674.1:g.111348722C>A GRCh37
NC_000012.10:g.109833105C>A NCBI36
NG_007554.1:g.14660G>T , LRG_393:g.14660G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000228841.15:c.*159G>T MANE Select ENSP00000228841.8:n.*159G>T
ENST00000663220.1:c.*159G>T ENSP00000499568.1:n.*159G>T
ENST00000228841.12:c.*159G>T ENSP00000228841.7:n.*159G>T
ENST00000548438.1:c.*159G>T ENSP00000447154.1:n.*159G>T
NM_000432.3:c.*159G>T , LRG_393t1:c.*159G>T NP_000423.2:n.*159G>T
NM_000432.4:c.*159G>T MANE Select NP_000423.2:n.*159G>T
Search 100 bp 5'
Search 100 bp 3'