Canonical Allele Identifier: CA683554648
Gene: MYL2 HGNC NCBI

Linked Data

dbSNP Id: rs1346510990

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.110911014A>C , CM000674.2:g.110911014A>C GRCh38
NC_000012.11:g.111348818A>C , CM000674.1:g.111348818A>C GRCh37
NC_000012.10:g.109833201A>C NCBI36
NG_007554.1:g.14564T>G , LRG_393:g.14564T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000228841.15:c.*63T>G MANE Select ENSP00000228841.8:n.*63T>G
ENST00000663220.1:c.*63T>G ENSP00000499568.1:n.*63T>G
ENST00000228841.12:c.*63T>G ENSP00000228841.7:n.*63T>G
ENST00000548438.1:c.*63T>G ENSP00000447154.1:n.*63T>G
NM_000432.3:c.*63T>G , LRG_393t1:c.*63T>G NP_000423.2:n.*63T>G
NM_000432.4:c.*63T>G MANE Select NP_000423.2:n.*63T>G