Canonical Allele Identifier: CA467496363
Gene: ABL1 HGNC NCBI

Linked Data

dbSNP Id: rs2132974040
MyVariant Identifiers: chr9:g.133738353C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130862966C>G , CM000671.2:g.130862966C>G GRCh38
NC_000009.11:g.133738353C>G , CM000671.1:g.133738353C>G GRCh37
NC_000009.10:g.132728174C>G NCBI36
NG_012034.1:g.154086C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000372348.9:c.810C>G ENSP00000361423.2:p.Gly270=
ENST00000318560.6:c.753C>G MANE Select ENSP00000323315.5:p.Gly251=
ENST00000372348.7:c.810C>G ENSP00000361423.2:p.Gly270=
ENST00000318560.5:c.753C>G ENSP00000323315.5:p.Gly251=
ENST00000372348.6:c.810C>G ENSP00000361423.2:p.Gly270=
NM_005157.5:c.753C>G NP_005148.2:p.Gly251=
NM_007313.2:c.810C>G NP_009297.2:p.Gly270=
NM_005157.6:c.753C>G MANE Select NP_005148.2:p.Gly251=
NM_007313.3:c.810C>G NP_009297.2:p.Gly270=