Canonical Allele Identifier: CA467496243
Gene: ABL1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.133738254A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130862867A>G , CM000671.2:g.130862867A>G GRCh38
NC_000009.11:g.133738254A>G , CM000671.1:g.133738254A>G GRCh37
NC_000009.10:g.132728075A>G NCBI36
NG_012034.1:g.153987A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000372348.9:c.711A>G ENSP00000361423.2:p.Pro237=
ENST00000318560.6:c.654A>G MANE Select ENSP00000323315.5:p.Pro218=
ENST00000372348.7:c.711A>G ENSP00000361423.2:p.Pro237=
ENST00000318560.5:c.654A>G ENSP00000323315.5:p.Pro218=
ENST00000372348.6:c.711A>G ENSP00000361423.2:p.Pro237=
NM_005157.5:c.654A>G NP_005148.2:p.Pro218=
NM_007313.2:c.711A>G NP_009297.2:p.Pro237=
NM_005157.6:c.654A>G MANE Select NP_005148.2:p.Pro218=
NM_007313.3:c.711A>G NP_009297.2:p.Pro237=