Canonical Allele Identifier: CA375249664
Gene: ABL1 HGNC NCBI

Linked Data

dbSNP Id: rs1362587735

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130873010A>C , CM000671.2:g.130873010A>C GRCh38
NC_000009.11:g.133748397A>C , CM000671.1:g.133748397A>C GRCh37
NC_000009.10:g.132738218A>C NCBI36
NG_012034.1:g.164130A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000372348.9:c.1115A>C ENSP00000361423.2:p.Tyr372Ser
ENST00000318560.6:c.1058A>C MANE Select ENSP00000323315.5:p.Tyr353Ser
ENST00000372348.7:c.1115A>C ENSP00000361423.2:p.Tyr372Ser
ENST00000318560.5:c.1058A>C ENSP00000323315.5:p.Tyr353Ser
ENST00000372348.6:c.1115A>C ENSP00000361423.2:p.Tyr372Ser
NM_005157.5:c.1058A>C NP_005148.2:p.Tyr353Ser
NM_007313.2:c.1115A>C NP_009297.2:p.Tyr372Ser
NM_005157.6:c.1058A>C MANE Select NP_005148.2:p.Tyr353Ser
NM_007313.3:c.1115A>C NP_009297.2:p.Tyr372Ser