Canonical Allele Identifier: CA1881476256
Gene: ABL1 HGNC NCBI

Linked Data

dbSNP Id: rs1831280439

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130873077G>C , CM000671.2:g.130873077G>C GRCh38
NC_000009.11:g.133748464G>C , CM000671.1:g.133748464G>C GRCh37
NC_000009.10:g.132738285G>C NCBI36
NG_012034.1:g.164197G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000372348.9:c.1142+40G>C ENSP00000361423.2:n.1142+40G>C
ENST00000318560.6:c.1085+40G>C MANE Select ENSP00000323315.5:n.1085+40G>C
ENST00000372348.7:c.1142+40G>C ENSP00000361423.2:n.1142+40G>C
ENST00000318560.5:c.1085+40G>C ENSP00000323315.5:n.1085+40G>C
ENST00000372348.6:c.1142+40G>C ENSP00000361423.2:n.1142+40G>C
NM_005157.5:c.1085+40G>C NP_005148.2:n.1085+40G>C
NM_007313.2:c.1142+40G>C NP_009297.2:n.1142+40G>C
NM_005157.6:c.1085+40G>C MANE Select NP_005148.2:n.1085+40G>C
NM_007313.3:c.1142+40G>C NP_009297.2:n.1142+40G>C