Canonical Allele Identifier: CA352495398

Gene: MYL3

Linked Data

• gnomAD v4: 3-46858413-T-A
• MyVariant Identifiers: chr3:g.46899903T>A (hg19) ; chr3:g.46858413T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46858413T>A , CM000665.2:g.46858413T>A	GRCh38
NC_000003.11:g.46899903T>A , CM000665.1:g.46899903T>A	GRCh37
NC_000003.10:g.46874907T>A	NCBI36
NG_007555.2:g.28757A>T , LRG_395:g.28757A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000431168.2:c.530A>T	ENSP00000393455.2:p.Glu177Val
ENST00000292327.6:c.530A>T MANE Select	ENSP00000292327.4:p.Glu177Val
ENST00000653454.1:c.530A>T	ENSP00000499624.1:p.Glu177Val
ENST00000654597.1:c.530A>T	ENSP00000499406.1:p.Glu177Val
ENST00000655244.1:n.737A>T
ENST00000662933.1:c.530A>T	ENSP00000499577.1:p.Glu177Val
ENST00000664891.1:n.488A>T
ENST00000292327.4:c.530A>T	ENSP00000292327.4:p.Glu177Val
ENST00000395869.5:c.530A>T	ENSP00000379210.1:p.Glu177Val
NM_000258.2:c.530A>T , LRG_395t1:c.530A>T	NP_000249.1:p.Glu177Val
NM_000258.3:c.530A>T MANE Select	NP_000249.1:p.Glu177Val