Canonical Allele Identifier: CA1881474981
Gene: ABL1 HGNC NCBI

Linked Data

dbSNP Id: rs1588276671

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130872499C>T , CM000671.2:g.130872499C>T GRCh38
NC_000009.11:g.133747886C>T , CM000671.1:g.133747886C>T GRCh37
NC_000009.10:g.132737707C>T NCBI36
NG_012034.1:g.163619C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000372348.9:c.964+286C>T ENSP00000361423.2:n.964+286C>T
ENST00000318560.6:c.907+286C>T MANE Select ENSP00000323315.5:n.907+286C>T
ENST00000372348.7:c.964+286C>T ENSP00000361423.2:n.964+286C>T
ENST00000318560.5:c.907+286C>T ENSP00000323315.5:n.907+286C>T
ENST00000372348.6:c.964+286C>T ENSP00000361423.2:n.964+286C>T
NM_005157.5:c.907+286C>T NP_005148.2:n.907+286C>T
NM_007313.2:c.964+286C>T NP_009297.2:n.964+286C>T
NM_005157.6:c.907+286C>T MANE Select NP_005148.2:n.907+286C>T
NM_007313.3:c.964+286C>T NP_009297.2:n.964+286C>T