Canonical Allele Identifier: CA1129551705
Gene: ABL1 HGNC NCBI

Linked Data

dbSNP Id: rs1831257379
gnomAD v3: 9-130871928-T-C
gnomAD v4: 9-130871928-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130871928T>C , CM000671.2:g.130871928T>C GRCh38
NC_000009.11:g.133747315T>C , CM000671.1:g.133747315T>C GRCh37
NC_000009.10:g.132737136T>C NCBI36
NG_012034.1:g.163048T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000372348.9:c.880-201T>C ENSP00000361423.2:n.880-201T>C
ENST00000318560.6:c.823-201T>C MANE Select ENSP00000323315.5:n.823-201T>C
ENST00000372348.7:c.880-201T>C ENSP00000361423.2:n.880-201T>C
ENST00000318560.5:c.823-201T>C ENSP00000323315.5:n.823-201T>C
ENST00000372348.6:c.880-201T>C ENSP00000361423.2:n.880-201T>C
NM_005157.5:c.823-201T>C NP_005148.2:n.823-201T>C
NM_007313.2:c.880-201T>C NP_009297.2:n.880-201T>C
NM_005157.6:c.823-201T>C MANE Select NP_005148.2:n.823-201T>C
NM_007313.3:c.880-201T>C NP_009297.2:n.880-201T>C
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