Canonical Allele Identifier: CA467496292
Gene: ABL1 HGNC NCBI

Linked Data

dbSNP Id: rs2132973837
MyVariant Identifiers: chr9:g.133738284G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130862897G>A , CM000671.2:g.130862897G>A GRCh38
NC_000009.11:g.133738284G>A , CM000671.1:g.133738284G>A GRCh37
NC_000009.10:g.132728105G>A NCBI36
NG_012034.1:g.154017G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000372348.9:c.741G>A ENSP00000361423.2:p.Val247=
ENST00000318560.6:c.684G>A MANE Select ENSP00000323315.5:p.Val228=
ENST00000372348.7:c.741G>A ENSP00000361423.2:p.Val247=
ENST00000318560.5:c.684G>A ENSP00000323315.5:p.Val228=
ENST00000372348.6:c.741G>A ENSP00000361423.2:p.Val247=
NM_005157.5:c.684G>A NP_005148.2:p.Val228=
NM_007313.2:c.741G>A NP_009297.2:p.Val247=
NM_005157.6:c.684G>A MANE Select NP_005148.2:p.Val228=
NM_007313.3:c.741G>A NP_009297.2:p.Val247=