Canonical Allele Identifier: CA860512314

Gene: ABL1

Linked Data

• dbSNP Id: rs1480492326
• gnomAD v3: 9-130873209-C-G
• gnomAD v4: 9-130873209-C-G
• MyVariant Identifiers: chr9:g.133748596C>G (hg19) ; chr9:g.130873209C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130873209C>G , CM000671.2:g.130873209C>G	GRCh38
NC_000009.11:g.133748596C>G , CM000671.1:g.133748596C>G	GRCh37
NC_000009.10:g.132738417C>G	NCBI36
NG_012034.1:g.164329C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372348.9:c.1142+172C>G	ENSP00000361423.2:n.1142+172C>G
ENST00000318560.6:c.1085+172C>G MANE Select	ENSP00000323315.5:n.1085+172C>G
ENST00000372348.7:c.1142+172C>G	ENSP00000361423.2:n.1142+172C>G
ENST00000318560.5:c.1085+172C>G	ENSP00000323315.5:n.1085+172C>G
ENST00000372348.6:c.1142+172C>G	ENSP00000361423.2:n.1142+172C>G
NM_005157.5:c.1085+172C>G	NP_005148.2:n.1085+172C>G
NM_007313.2:c.1142+172C>G	NP_009297.2:n.1142+172C>G
NM_005157.6:c.1085+172C>G MANE Select	NP_005148.2:n.1085+172C>G
NM_007313.3:c.1142+172C>G	NP_009297.2:n.1142+172C>G