Canonical Allele Identifier: CA2692152485
Gene: ABL1 HGNC NCBI

Linked Data

gnomAD v4: 9-130872032-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130872032A>G , CM000671.2:g.130872032A>G GRCh38
NC_000009.11:g.133747419A>G , CM000671.1:g.133747419A>G GRCh37
NC_000009.10:g.132737240A>G NCBI36
NG_012034.1:g.163152A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000372348.9:c.880-97A>G ENSP00000361423.2:n.880-97A>G
ENST00000318560.6:c.823-97A>G MANE Select ENSP00000323315.5:n.823-97A>G
ENST00000372348.7:c.880-97A>G ENSP00000361423.2:n.880-97A>G
ENST00000318560.5:c.823-97A>G ENSP00000323315.5:n.823-97A>G
ENST00000372348.6:c.880-97A>G ENSP00000361423.2:n.880-97A>G
NM_005157.5:c.823-97A>G NP_005148.2:n.823-97A>G
NM_007313.2:c.880-97A>G NP_009297.2:n.880-97A>G
NM_005157.6:c.823-97A>G MANE Select NP_005148.2:n.823-97A>G
NM_007313.3:c.880-97A>G NP_009297.2:n.880-97A>G
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