Canonical Allele Identifier: CA467395117
Gene: ABL1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.133748323G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130872936G>A , CM000671.2:g.130872936G>A GRCh38
NC_000009.11:g.133748323G>A , CM000671.1:g.133748323G>A GRCh37
NC_000009.10:g.132738144G>A NCBI36
NG_012034.1:g.164056G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000372348.9:c.1041G>A ENSP00000361423.2:p.Arg347=
ENST00000318560.6:c.984G>A MANE Select ENSP00000323315.5:p.Arg328=
ENST00000372348.7:c.1041G>A ENSP00000361423.2:p.Arg347=
ENST00000318560.5:c.984G>A ENSP00000323315.5:p.Arg328=
ENST00000372348.6:c.1041G>A ENSP00000361423.2:p.Arg347=
NM_005157.5:c.984G>A NP_005148.2:p.Arg328=
NM_007313.2:c.1041G>A NP_009297.2:p.Arg347=
NM_005157.6:c.984G>A MANE Select NP_005148.2:p.Arg328=
NM_007313.3:c.1041G>A NP_009297.2:p.Arg347=