Canonical Allele Identifier: CA860511174
Gene: ABL1 HGNC NCBI

Linked Data

dbSNP Id: rs1355338453

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130872023A>G , CM000671.2:g.130872023A>G GRCh38
NC_000009.11:g.133747410A>G , CM000671.1:g.133747410A>G GRCh37
NC_000009.10:g.132737231A>G NCBI36
NG_012034.1:g.163143A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000372348.9:c.880-106A>G ENSP00000361423.2:n.880-106A>G
ENST00000318560.6:c.823-106A>G MANE Select ENSP00000323315.5:n.823-106A>G
ENST00000372348.7:c.880-106A>G ENSP00000361423.2:n.880-106A>G
ENST00000318560.5:c.823-106A>G ENSP00000323315.5:n.823-106A>G
ENST00000372348.6:c.880-106A>G ENSP00000361423.2:n.880-106A>G
NM_005157.5:c.823-106A>G NP_005148.2:n.823-106A>G
NM_007313.2:c.880-106A>G NP_009297.2:n.880-106A>G
NM_005157.6:c.823-106A>G MANE Select NP_005148.2:n.823-106A>G
NM_007313.3:c.880-106A>G NP_009297.2:n.880-106A>G