Canonical Allele Identifier: CA386697815
Gene: MYL2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.111350949C>T (hg19) chr12:g.110913145C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.110913145C>T , CM000674.2:g.110913145C>T GRCh38
NC_000012.11:g.111350949C>T , CM000674.1:g.111350949C>T GRCh37
NC_000012.10:g.109835332C>T NCBI36
NG_007554.1:g.12433G>A , LRG_393:g.12433G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000228841.15:c.354-1G>A MANE Select ENSP00000228841.8:n.354-1G>A
ENST00000663220.1:c.297-1G>A ENSP00000499568.1:n.297-1G>A
ENST00000228841.12:c.354-1G>A ENSP00000228841.7:n.354-1G>A
ENST00000548438.1:c.312-1G>A ENSP00000447154.1:n.312-1G>A
ENST00000549029.1:n.285G>A
NM_000432.3:c.354-1G>A , LRG_393t1:c.354-1G>A NP_000423.2:n.354-1G>A
NM_000432.4:c.354-1G>A MANE Select NP_000423.2:n.354-1G>A
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