Canonical Allele Identifier: CA467395179

Gene: ABL1

Linked Data

• dbSNP Id: rs1831278899
• MyVariant Identifiers: chr9:g.133748380C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130872993C>T , CM000671.2:g.130872993C>T	GRCh38
NC_000009.11:g.133748380C>T , CM000671.1:g.133748380C>T	GRCh37
NC_000009.10:g.132738201C>T	NCBI36
NG_012034.1:g.164113C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372348.9:c.1098C>T	ENSP00000361423.2:p.Ile366=
ENST00000318560.6:c.1041C>T MANE Select	ENSP00000323315.5:p.Ile347=
ENST00000372348.7:c.1098C>T	ENSP00000361423.2:p.Ile366=
ENST00000318560.5:c.1041C>T	ENSP00000323315.5:p.Ile347=
ENST00000372348.6:c.1098C>T	ENSP00000361423.2:p.Ile366=
NM_005157.5:c.1041C>T	NP_005148.2:p.Ile347=
NM_007313.2:c.1098C>T	NP_009297.2:p.Ile366=
NM_005157.6:c.1041C>T MANE Select	NP_005148.2:p.Ile347=
NM_007313.3:c.1098C>T	NP_009297.2:p.Ile366=