Canonical Allele Identifier: CA467395156
Gene: ABL1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.133748357C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130872970C>T , CM000671.2:g.130872970C>T GRCh38
NC_000009.11:g.133748357C>T , CM000671.1:g.133748357C>T GRCh37
NC_000009.10:g.132738178C>T NCBI36
NG_012034.1:g.164090C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000372348.9:c.1075C>T ENSP00000361423.2:p.Leu359=
ENST00000318560.6:c.1018C>T MANE Select ENSP00000323315.5:p.Leu340=
ENST00000372348.7:c.1075C>T ENSP00000361423.2:p.Leu359=
ENST00000318560.5:c.1018C>T ENSP00000323315.5:p.Leu340=
ENST00000372348.6:c.1075C>T ENSP00000361423.2:p.Leu359=
NM_005157.5:c.1018C>T NP_005148.2:p.Leu340=
NM_007313.2:c.1075C>T NP_009297.2:p.Leu359=
NM_005157.6:c.1018C>T MANE Select NP_005148.2:p.Leu340=
NM_007313.3:c.1075C>T NP_009297.2:p.Leu359=