Canonical Allele Identifier: CA467496170

Gene: ABL1

Linked Data

• MyVariant Identifiers: chr9:g.133738161C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130862774C>G , CM000671.2:g.130862774C>G	GRCh38
NC_000009.11:g.133738161C>G , CM000671.1:g.133738161C>G	GRCh37
NC_000009.10:g.132727982C>G	NCBI36
NG_012034.1:g.153894C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000372348.9:c.618C>G	ENSP00000361423.2:p.Ser206=
ENST00000318560.6:c.561C>G MANE Select	ENSP00000323315.5:p.Ser187=
ENST00000372348.7:c.618C>G	ENSP00000361423.2:p.Ser206=
ENST00000318560.5:c.561C>G	ENSP00000323315.5:p.Ser187=
ENST00000372348.6:c.618C>G	ENSP00000361423.2:p.Ser206=
NM_005157.5:c.561C>G	NP_005148.2:p.Ser187=
NM_007313.2:c.618C>G	NP_009297.2:p.Ser206=
NM_005157.6:c.561C>G MANE Select	NP_005148.2:p.Ser187=
NM_007313.3:c.618C>G	NP_009297.2:p.Ser206=