Canonical Allele Identifier: CA433474566

Gene: MYL3

Linked Data

• ClinVar Variation Id: 3075509
• ClinVar RCV Id: RCV004017027
• dbSNP Id: rs761891361
• gnomAD v2: 3-46902232-G-T
• gnomAD v4: 3-46860742-G-T
• MyVariant Identifiers: chr3:g.46902232G>T (hg19) ; chr3:g.46860742G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46860742G>T , CM000665.2:g.46860742G>T	GRCh38
NC_000003.11:g.46902232G>T , CM000665.1:g.46902232G>T	GRCh37
NC_000003.10:g.46877236G>T	NCBI36
NG_007555.2:g.26428C>A , LRG_395:g.26428C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000431168.2:c.241C>A	ENSP00000393455.2:p.Arg81=
ENST00000292327.6:c.241C>A MANE Select	ENSP00000292327.4:p.Arg81=
ENST00000653454.1:c.241C>A	ENSP00000499624.1:p.Arg81=
ENST00000654597.1:c.241C>A	ENSP00000499406.1:p.Arg81=
ENST00000655244.1:n.463C>A
ENST00000662933.1:c.241C>A	ENSP00000499577.1:p.Arg81=
ENST00000664891.1:n.199C>A
ENST00000292327.4:c.241C>A	ENSP00000292327.4:p.Arg81=
ENST00000395869.5:c.241C>A	ENSP00000379210.1:p.Arg81=
NM_000258.2:c.241C>A , LRG_395t1:c.241C>A	NP_000249.1:p.Arg81=
NM_000258.3:c.241C>A MANE Select	NP_000249.1:p.Arg81=