Canonical Allele Identifier: CA200645209

Gene: ABL1

Linked Data

• dbSNP Id: rs977039326
• gnomAD v2: 9-133747753-G-T
• gnomAD v3: 9-130872366-G-T
• gnomAD v4: 9-130872366-G-T
• MyVariant Identifiers: chr9:g.133747753G>T (hg19) ; chr9:g.130872366G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130872366G>T , CM000671.2:g.130872366G>T	GRCh38
NC_000009.11:g.133747753G>T , CM000671.1:g.133747753G>T	GRCh37
NC_000009.10:g.132737574G>T	NCBI36
NG_012034.1:g.163486G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372348.9:c.964+153G>T	ENSP00000361423.2:n.964+153G>T
ENST00000318560.6:c.907+153G>T MANE Select	ENSP00000323315.5:n.907+153G>T
ENST00000372348.7:c.964+153G>T	ENSP00000361423.2:n.964+153G>T
ENST00000318560.5:c.907+153G>T	ENSP00000323315.5:n.907+153G>T
ENST00000372348.6:c.964+153G>T	ENSP00000361423.2:n.964+153G>T
NM_005157.5:c.907+153G>T	NP_005148.2:n.907+153G>T
NM_007313.2:c.964+153G>T	NP_009297.2:n.964+153G>T
NM_005157.6:c.907+153G>T MANE Select	NP_005148.2:n.907+153G>T
NM_007313.3:c.964+153G>T	NP_009297.2:n.964+153G>T