Canonical Allele Identifier: CA1474633754
Gene: ABCG2 HGNC NCBI

Linked Data

dbSNP Id: rs1727679384

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88169704_88169707del , CM000666.2:g.88169704_88169707del GRCh38
NC_000004.11:g.89090856_89090859del , CM000666.1:g.89090856_89090859del GRCh37
NC_000004.10:g.89309880_89309883del NCBI36
NG_032067.2:g.66622_66625del

Transcript Alleles

HGVS Amino-acid Change
ENST00000650821.1:c.-19-29687_-19-29684del ENSP00000498246.1:n.-19-29687_-19-29684del
ENST00000515655.5:c.-19-29687_-19-29684del ENSP00000426917.1:n.-19-29687_-19-29684del
NM_001257386.1:c.-19-29687_-19-29684del NP_001244315.1:n.-19-29687_-19-29684del
XM_005263355.2:c.-19-29687_-19-29684del XP_005263412.1:n.-19-29687_-19-29684del
XM_011532420.1:c.-19-29687_-19-29684del XP_011530722.1:n.-19-29687_-19-29684del
NM_001257386.2:c.-19-29687_-19-29684del NP_001244315.1:n.-19-29687_-19-29684del
NM_001348985.1:c.-19-29687_-19-29684del NP_001335914.1:n.-19-29687_-19-29684del
XM_005263355.4:c.-19-29687_-19-29684del XP_005263412.1:n.-19-29687_-19-29684del
XM_011532420.3:c.-19-29687_-19-29684del XP_011530722.1:n.-19-29687_-19-29684del