Canonical Allele Identifier: CA100899921
Gene: ABCG2 HGNC NCBI

Linked Data

dbSNP Id: rs998965605

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88169659_88169662del , CM000666.2:g.88169659_88169662del GRCh38
NC_000004.11:g.89090811_89090814del , CM000666.1:g.89090811_89090814del GRCh37
NC_000004.10:g.89309835_89309838del NCBI36
NG_032067.2:g.66667_66670del

Transcript Alleles

HGVS Amino-acid change
ENST00000650821.1:c.-19-29642_-19-29639del ENSP00000498246.1:n.-19-29642_-19-29639de...
ENST00000515655.5:c.-19-29642_-19-29639del ENSP00000426917.1:n.-19-29642_-19-29639de...
NM_001257386.1:c.-19-29642_-19-29639del NP_001244315.1:n.-19-29642_-19-29639del
XM_005263355.2:c.-19-29642_-19-29639del XP_005263412.1:n.-19-29642_-19-29639del
XM_011532420.1:c.-19-29642_-19-29639del XP_011530722.1:n.-19-29642_-19-29639del
NM_001257386.2:c.-19-29642_-19-29639del NP_001244315.1:n.-19-29642_-19-29639del
NM_001348985.1:c.-19-29642_-19-29639del NP_001335914.1:n.-19-29642_-19-29639del
XM_005263355.4:c.-19-29642_-19-29639del XP_005263412.1:n.-19-29642_-19-29639del
XM_011532420.3:c.-19-29642_-19-29639del XP_011530722.1:n.-19-29642_-19-29639del