Canonical Allele Identifier: CA375262327
Gene: ABL1 HGNC NCBI

Linked Data

dbSNP Id: rs2132973184

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130862781A>T , CM000671.2:g.130862781A>T GRCh38
NC_000009.11:g.133738168A>T , CM000671.1:g.133738168A>T GRCh37
NC_000009.10:g.132727989A>T NCBI36
NG_012034.1:g.153901A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000372348.9:c.625A>T ENSP00000361423.2:p.Ser209Cys
ENST00000318560.6:c.568A>T MANE Select ENSP00000323315.5:p.Ser190Cys
ENST00000372348.7:c.625A>T ENSP00000361423.2:p.Ser209Cys
ENST00000318560.5:c.568A>T ENSP00000323315.5:p.Ser190Cys
ENST00000372348.6:c.625A>T ENSP00000361423.2:p.Ser209Cys
NM_005157.5:c.568A>T NP_005148.2:p.Ser190Cys
NM_007313.2:c.625A>T NP_009297.2:p.Ser209Cys
NM_005157.6:c.568A>T MANE Select NP_005148.2:p.Ser190Cys
NM_007313.3:c.625A>T NP_009297.2:p.Ser209Cys