Canonical Allele Identifier: CA481750995
Gene: MYL2 HGNC NCBI

Linked Data

gnomAD v4: 12-110914199-C-T
COSMIC: COSM4538915
MyVariant Identifiers: chr12:g.111352003C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.110914199C>T , CM000674.2:g.110914199C>T GRCh38
NC_000012.11:g.111352003C>T , CM000674.1:g.111352003C>T GRCh37
NC_000012.10:g.109836386C>T NCBI36
NG_007554.1:g.11379G>A , LRG_393:g.11379G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000228841.15:c.261G>A MANE Select ENSP00000228841.8:p.Gly87=
ENST00000663220.1:c.204G>A ENSP00000499568.1:p.Gly68=
ENST00000228841.12:c.261G>A ENSP00000228841.7:p.Gly87=
ENST00000548438.1:c.219G>A ENSP00000447154.1:p.Gly73=
ENST00000549029.1:n.92G>A
NM_000432.3:c.261G>A , LRG_393t1:c.261G>A NP_000423.2:p.Gly87=
NM_000432.4:c.261G>A MANE Select NP_000423.2:p.Gly87=
Search 100 bp 5'
Search 100 bp 3'