Canonical Allele Identifier: CA433474373

Gene: MYL3

Linked Data

• ClinVar Variation Id: 1741117
• ClinVar RCV Id: RCV002339909 ; RCV003748393
• dbSNP Id: rs1401349000
• gnomAD v3: 3-46859506-A-G
• gnomAD v4: 3-46859506-A-G
• MyVariant Identifiers: chr3:g.46900996A>G (hg19) ; chr3:g.46859506A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46859506A>G , CM000665.2:g.46859506A>G	GRCh38
NC_000003.11:g.46900996A>G , CM000665.1:g.46900996A>G	GRCh37
NC_000003.10:g.46876000A>G	NCBI36
NG_007555.2:g.27664T>C , LRG_395:g.27664T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000431168.2:c.450T>C	ENSP00000393455.2:p.Gly150=
ENST00000292327.6:c.450T>C MANE Select	ENSP00000292327.4:p.Gly150=
ENST00000653454.1:c.450T>C	ENSP00000499624.1:p.Gly150=
ENST00000654597.1:c.450T>C	ENSP00000499406.1:p.Gly150=
ENST00000655244.1:n.672T>C
ENST00000662933.1:c.450T>C	ENSP00000499577.1:p.Gly150=
ENST00000664891.1:n.408T>C
ENST00000292327.4:c.450T>C	ENSP00000292327.4:p.Gly150=
ENST00000395869.5:c.450T>C	ENSP00000379210.1:p.Gly150=
NM_000258.2:c.450T>C , LRG_395t1:c.450T>C	NP_000249.1:p.Gly150=
NM_000258.3:c.450T>C MANE Select	NP_000249.1:p.Gly150=