Canonical Allele Identifier: CA467496299

Gene: ABL1

Linked Data

• dbSNP Id: rs1307010569
• MyVariant Identifiers: chr9:g.133738287C>T (hg19) ; chr9:g.130862900C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130862900C>T , CM000671.2:g.130862900C>T	GRCh38
NC_000009.11:g.133738287C>T , CM000671.1:g.133738287C>T	GRCh37
NC_000009.10:g.132728108C>T	NCBI36
NG_012034.1:g.154020C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372348.9:c.744C>T	ENSP00000361423.2:p.Ser248=
ENST00000318560.6:c.687C>T MANE Select	ENSP00000323315.5:p.Ser229=
ENST00000372348.7:c.744C>T	ENSP00000361423.2:p.Ser248=
ENST00000318560.5:c.687C>T	ENSP00000323315.5:p.Ser229=
ENST00000372348.6:c.744C>T	ENSP00000361423.2:p.Ser248=
NM_005157.5:c.687C>T	NP_005148.2:p.Ser229=
NM_007313.2:c.744C>T	NP_009297.2:p.Ser248=
NM_005157.6:c.687C>T MANE Select	NP_005148.2:p.Ser229=
NM_007313.3:c.744C>T	NP_009297.2:p.Ser248=