Canonical Allele Identifier: CA352498267

Gene: MYL3

Linked Data

• ClinVar Variation Id: 629011
• ClinVar RCV Id: RCV000773697
• dbSNP Id: rs1559520411
• MyVariant Identifiers: chr3:g.46902244C>T (hg19) ; chr3:g.46860754C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46860754C>T , CM000665.2:g.46860754C>T	GRCh38
NC_000003.11:g.46902244C>T , CM000665.1:g.46902244C>T	GRCh37
NC_000003.10:g.46877248C>T	NCBI36
NG_007555.2:g.26416G>A , LRG_395:g.26416G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000431168.2:c.229G>A	ENSP00000393455.2:p.Gly77Arg
ENST00000292327.6:c.229G>A MANE Select	ENSP00000292327.4:p.Gly77Arg
ENST00000653454.1:c.229G>A	ENSP00000499624.1:p.Gly77Arg
ENST00000654597.1:c.229G>A	ENSP00000499406.1:p.Gly77Arg
ENST00000655244.1:n.451G>A
ENST00000662933.1:c.229G>A	ENSP00000499577.1:p.Gly77Arg
ENST00000664891.1:n.187G>A
ENST00000292327.4:c.229G>A	ENSP00000292327.4:p.Gly77Arg
ENST00000395869.5:c.229G>A	ENSP00000379210.1:p.Gly77Arg
NM_000258.2:c.229G>A , LRG_395t1:c.229G>A	NP_000249.1:p.Gly77Arg
NM_000258.3:c.229G>A MANE Select	NP_000249.1:p.Gly77Arg