Canonical Allele Identifier: CA2720749365
Gene: ABL1 HGNC NCBI

Linked Data

dbSNP Id: rs2132997855

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130873072T>A , CM000671.2:g.130873072T>A GRCh38
NC_000009.11:g.133748459T>A , CM000671.1:g.133748459T>A GRCh37
NC_000009.10:g.132738280T>A NCBI36
NG_012034.1:g.164192T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000372348.9:c.1142+35T>A ENSP00000361423.2:n.1142+35T>A
ENST00000318560.6:c.1085+35T>A MANE Select ENSP00000323315.5:n.1085+35T>A
ENST00000372348.7:c.1142+35T>A ENSP00000361423.2:n.1142+35T>A
ENST00000318560.5:c.1085+35T>A ENSP00000323315.5:n.1085+35T>A
ENST00000372348.6:c.1142+35T>A ENSP00000361423.2:n.1142+35T>A
NM_005157.5:c.1085+35T>A NP_005148.2:n.1085+35T>A
NM_007313.2:c.1142+35T>A NP_009297.2:n.1142+35T>A
NM_005157.6:c.1085+35T>A MANE Select NP_005148.2:n.1085+35T>A
NM_007313.3:c.1142+35T>A NP_009297.2:n.1142+35T>A