Canonical Allele Identifier: CA044855

Gene: MYL3

Linked Data

• dbSNP Id: rs751286084
• ExAC: 3:46899834 C / A
• gnomAD v2: 3-46899834-C-A
• MyVariant Identifiers: chr3:g.46899834C>A (hg19) ; chr3:g.46858344C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46858344C>A , CM000665.2:g.46858344C>A	GRCh38
NC_000003.11:g.46899834C>A , CM000665.1:g.46899834C>A	GRCh37
NC_000003.10:g.46874838C>A	NCBI36
NG_007555.2:g.28826G>T , LRG_395:g.28826G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000431168.2:c.559+40G>T	ENSP00000393455.2:n.559+40G>T
ENST00000292327.6:c.559+40G>T MANE Select	ENSP00000292327.4:n.559+40G>T
ENST00000653454.1:c.559+40G>T	ENSP00000499624.1:n.559+40G>T
ENST00000654597.1:c.559+40G>T	ENSP00000499406.1:n.559+40G>T
ENST00000655244.1:n.766+40G>T
ENST00000662933.1:c.559+40G>T	ENSP00000499577.1:n.559+40G>T
ENST00000664891.1:n.517+40G>T
ENST00000292327.4:c.559+40G>T	ENSP00000292327.4:n.559+40G>T
ENST00000395869.5:c.559+40G>T	ENSP00000379210.1:n.559+40G>T
NM_000258.2:c.559+40G>T , LRG_395t1:c.559+40G>T	NP_000249.1:n.559+40G>T
NM_000258.3:c.559+40G>T MANE Select	NP_000249.1:n.559+40G>T