Canonical Allele Identifier: CA467395038

Gene: ABL1

Linked Data

• gnomAD v4: 9-130872870-C-T
• MyVariant Identifiers: chr9:g.133748257C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130872870C>T , CM000671.2:g.130872870C>T	GRCh38
NC_000009.11:g.133748257C>T , CM000671.1:g.133748257C>T	GRCh37
NC_000009.10:g.132738078C>T	NCBI36
NG_012034.1:g.163990C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372348.9:c.975C>T	ENSP00000361423.2:p.Thr325=
ENST00000318560.6:c.918C>T MANE Select	ENSP00000323315.5:p.Thr306=
ENST00000372348.7:c.975C>T	ENSP00000361423.2:p.Thr325=
ENST00000318560.5:c.918C>T	ENSP00000323315.5:p.Thr306=
ENST00000372348.6:c.975C>T	ENSP00000361423.2:p.Thr325=
NM_005157.5:c.918C>T	NP_005148.2:p.Thr306=
NM_007313.2:c.975C>T	NP_009297.2:p.Thr325=
NM_005157.6:c.918C>T MANE Select	NP_005148.2:p.Thr306=
NM_007313.3:c.975C>T	NP_009297.2:p.Thr325=