Canonical Allele Identifier: CA860512249

Gene: ABL1

Linked Data

• dbSNP Id: rs1016909312
• gnomAD v3: 9-130873108-G-T
• gnomAD v4: 9-130873108-G-T
• MyVariant Identifiers: chr9:g.133748495G>T (hg19) ; chr9:g.130873108G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130873108G>T , CM000671.2:g.130873108G>T	GRCh38
NC_000009.11:g.133748495G>T , CM000671.1:g.133748495G>T	GRCh37
NC_000009.10:g.132738316G>T	NCBI36
NG_012034.1:g.164228G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372348.9:c.1142+71G>T	ENSP00000361423.2:n.1142+71G>T
ENST00000318560.6:c.1085+71G>T MANE Select	ENSP00000323315.5:n.1085+71G>T
ENST00000372348.7:c.1142+71G>T	ENSP00000361423.2:n.1142+71G>T
ENST00000318560.5:c.1085+71G>T	ENSP00000323315.5:n.1085+71G>T
ENST00000372348.6:c.1142+71G>T	ENSP00000361423.2:n.1142+71G>T
NM_005157.5:c.1085+71G>T	NP_005148.2:n.1085+71G>T
NM_007313.2:c.1142+71G>T	NP_009297.2:n.1142+71G>T
NM_005157.6:c.1085+71G>T MANE Select	NP_005148.2:n.1085+71G>T
NM_007313.3:c.1142+71G>T	NP_009297.2:n.1142+71G>T