Canonical Allele Identifier: CA200644941

Gene: ABL1

Linked Data

• dbSNP Id: rs576699626
• gnomAD v3: 9-130871913-G-A
• gnomAD v4: 9-130871913-G-A
• MyVariant Identifiers: chr9:g.133747300G>A (hg19) ; chr9:g.130871913G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130871913G>A , CM000671.2:g.130871913G>A	GRCh38
NC_000009.11:g.133747300G>A , CM000671.1:g.133747300G>A	GRCh37
NC_000009.10:g.132737121G>A	NCBI36
NG_012034.1:g.163033G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372348.9:c.880-216G>A	ENSP00000361423.2:n.880-216G>A
ENST00000318560.6:c.823-216G>A MANE Select	ENSP00000323315.5:n.823-216G>A
ENST00000372348.7:c.880-216G>A	ENSP00000361423.2:n.880-216G>A
ENST00000318560.5:c.823-216G>A	ENSP00000323315.5:n.823-216G>A
ENST00000372348.6:c.880-216G>A	ENSP00000361423.2:n.880-216G>A
NM_005157.5:c.823-216G>A	NP_005148.2:n.823-216G>A
NM_007313.2:c.880-216G>A	NP_009297.2:n.880-216G>A
NM_005157.6:c.823-216G>A MANE Select	NP_005148.2:n.823-216G>A
NM_007313.3:c.880-216G>A	NP_009297.2:n.880-216G>A