Canonical Allele Identifier: CA2620917301
Gene: MYL2 HGNC NCBI

Linked Data

gnomAD v4: 12-110914387-A-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.110914387A>G , CM000674.2:g.110914387A>G GRCh38
NC_000012.11:g.111352191A>G , CM000674.1:g.111352191A>G GRCh37
NC_000012.10:g.109836574A>G NCBI36
NG_007554.1:g.11191T>C , LRG_393:g.11191T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000228841.15:c.170-97T>C MANE Select ENSP00000228841.8:n.170-97T>C
ENST00000663220.1:c.113-97T>C ENSP00000499568.1:n.113-97T>C
ENST00000228841.12:c.170-97T>C ENSP00000228841.7:n.170-97T>C
ENST00000548438.1:c.94-63T>C ENSP00000447154.1:n.94-63T>C
NM_000432.3:c.170-97T>C , LRG_393t1:c.170-97T>C NP_000423.2:n.170-97T>C
NM_000432.4:c.170-97T>C MANE Select NP_000423.2:n.170-97T>C
Search 100 bp 5'
Search 100 bp 3'