Canonical Allele Identifier: CA467496359
Gene: ABL1 HGNC NCBI

Linked Data

dbSNP Id: rs781647687

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130862963G>T , CM000671.2:g.130862963G>T GRCh38
NC_000009.11:g.133738350G>T , CM000671.1:g.133738350G>T GRCh37
NC_000009.10:g.132728171G>T NCBI36
NG_012034.1:g.154083G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000372348.9:c.807G>T ENSP00000361423.2:p.Gly269=
ENST00000318560.6:c.750G>T MANE Select ENSP00000323315.5:p.Gly250=
ENST00000372348.7:c.807G>T ENSP00000361423.2:p.Gly269=
ENST00000318560.5:c.750G>T ENSP00000323315.5:p.Gly250=
ENST00000372348.6:c.807G>T ENSP00000361423.2:p.Gly269=
NM_005157.5:c.750G>T NP_005148.2:p.Gly250=
NM_007313.2:c.807G>T NP_009297.2:p.Gly269=
NM_005157.6:c.750G>T MANE Select NP_005148.2:p.Gly250=
NM_007313.3:c.807G>T NP_009297.2:p.Gly269=