Canonical Allele Identifier: CA1881474478
Gene: ABL1 HGNC NCBI

Linked Data

dbSNP Id: rs1831256463

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130871862C>T , CM000671.2:g.130871862C>T GRCh38
NC_000009.11:g.133747249C>T , CM000671.1:g.133747249C>T GRCh37
NC_000009.10:g.132737070C>T NCBI36
NG_012034.1:g.162982C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000372348.9:c.880-267C>T ENSP00000361423.2:n.880-267C>T
ENST00000318560.6:c.823-267C>T MANE Select ENSP00000323315.5:n.823-267C>T
ENST00000372348.7:c.880-267C>T ENSP00000361423.2:n.880-267C>T
ENST00000318560.5:c.823-267C>T ENSP00000323315.5:n.823-267C>T
ENST00000372348.6:c.880-267C>T ENSP00000361423.2:n.880-267C>T
NM_005157.5:c.823-267C>T NP_005148.2:n.823-267C>T
NM_007313.2:c.880-267C>T NP_009297.2:n.880-267C>T
NM_005157.6:c.823-267C>T MANE Select NP_005148.2:n.823-267C>T
NM_007313.3:c.880-267C>T NP_009297.2:n.880-267C>T