Canonical Allele Identifier: CA375262378
Gene: ABL1 HGNC NCBI

Linked Data

dbSNP Id: rs1588272569

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130862793A>G , CM000671.2:g.130862793A>G GRCh38
NC_000009.11:g.133738180A>G , CM000671.1:g.133738180A>G GRCh37
NC_000009.10:g.132728001A>G NCBI36
NG_012034.1:g.153913A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000372348.9:c.637A>G ENSP00000361423.2:p.Thr213Ala
ENST00000318560.6:c.580A>G MANE Select ENSP00000323315.5:p.Thr194Ala
ENST00000372348.7:c.637A>G ENSP00000361423.2:p.Thr213Ala
ENST00000318560.5:c.580A>G ENSP00000323315.5:p.Thr194Ala
ENST00000372348.6:c.637A>G ENSP00000361423.2:p.Thr213Ala
NM_005157.5:c.580A>G NP_005148.2:p.Thr194Ala
NM_007313.2:c.637A>G NP_009297.2:p.Thr213Ala
NM_005157.6:c.580A>G MANE Select NP_005148.2:p.Thr194Ala
NM_007313.3:c.637A>G NP_009297.2:p.Thr213Ala