Canonical Allele Identifier: CA1129551975
Gene: ABL1 HGNC NCBI

Linked Data

dbSNP Id: rs1178729788
gnomAD v3: 9-130872742-G-C
gnomAD v4: 9-130872742-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130872742G>C , CM000671.2:g.130872742G>C GRCh38
NC_000009.11:g.133748129G>C , CM000671.1:g.133748129G>C GRCh37
NC_000009.10:g.132737950G>C NCBI36
NG_012034.1:g.163862G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000372348.9:c.965-118G>C ENSP00000361423.2:n.965-118G>C
ENST00000318560.6:c.908-118G>C MANE Select ENSP00000323315.5:n.908-118G>C
ENST00000372348.7:c.965-118G>C ENSP00000361423.2:n.965-118G>C
ENST00000318560.5:c.908-118G>C ENSP00000323315.5:n.908-118G>C
ENST00000372348.6:c.965-118G>C ENSP00000361423.2:n.965-118G>C
NM_005157.5:c.908-118G>C NP_005148.2:n.908-118G>C
NM_007313.2:c.965-118G>C NP_009297.2:n.965-118G>C
NM_005157.6:c.908-118G>C MANE Select NP_005148.2:n.908-118G>C
NM_007313.3:c.965-118G>C NP_009297.2:n.965-118G>C
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