Canonical Allele Identifier: CA375263100
Gene: ABL1 HGNC NCBI

Linked Data

dbSNP Id: rs2132973943

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130862938T>C , CM000671.2:g.130862938T>C GRCh38
NC_000009.11:g.133738325T>C , CM000671.1:g.133738325T>C GRCh37
NC_000009.10:g.132728146T>C NCBI36
NG_012034.1:g.154058T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000372348.9:c.782T>C ENSP00000361423.2:p.Ile261Thr
ENST00000318560.6:c.725T>C MANE Select ENSP00000323315.5:p.Ile242Thr
ENST00000372348.7:c.782T>C ENSP00000361423.2:p.Ile261Thr
ENST00000318560.5:c.725T>C ENSP00000323315.5:p.Ile242Thr
ENST00000372348.6:c.782T>C ENSP00000361423.2:p.Ile261Thr
NM_005157.5:c.725T>C NP_005148.2:p.Ile242Thr
NM_007313.2:c.782T>C NP_009297.2:p.Ile261Thr
NM_005157.6:c.725T>C MANE Select NP_005148.2:p.Ile242Thr
NM_007313.3:c.782T>C NP_009297.2:p.Ile261Thr