Canonical Allele Identifier: CA590717903

Gene: ABL1

Linked Data

• dbSNP Id: rs1310555969
• gnomAD v2: 9-133748011-G-C
• gnomAD v3: 9-130872624-G-C
• gnomAD v4: 9-130872624-G-C
• MyVariant Identifiers: chr9:g.133748011G>C (hg19) ; chr9:g.130872624G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130872624G>C , CM000671.2:g.130872624G>C	GRCh38
NC_000009.11:g.133748011G>C , CM000671.1:g.133748011G>C	GRCh37
NC_000009.10:g.132737832G>C	NCBI36
NG_012034.1:g.163744G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372348.9:c.965-236G>C	ENSP00000361423.2:n.965-236G>C
ENST00000318560.6:c.908-236G>C MANE Select	ENSP00000323315.5:n.908-236G>C
ENST00000372348.7:c.965-236G>C	ENSP00000361423.2:n.965-236G>C
ENST00000318560.5:c.908-236G>C	ENSP00000323315.5:n.908-236G>C
ENST00000372348.6:c.965-236G>C	ENSP00000361423.2:n.965-236G>C
NM_005157.5:c.908-236G>C	NP_005148.2:n.908-236G>C
NM_007313.2:c.965-236G>C	NP_009297.2:n.965-236G>C
NM_005157.6:c.908-236G>C MANE Select	NP_005148.2:n.908-236G>C
NM_007313.3:c.965-236G>C	NP_009297.2:n.965-236G>C