Canonical Allele Identifier: CA1065137865
Gene: ABCG2 HGNC NCBI

Linked Data

dbSNP Id: rs1727673997

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88169552_88169553del , CM000666.2:g.88169552_88169553del GRCh38
NC_000004.11:g.89090704_89090705del , CM000666.1:g.89090704_89090705del GRCh37
NC_000004.10:g.89309728_89309729del NCBI36
NG_032067.2:g.66772_66773del

Transcript Alleles

HGVS Amino-acid Change
ENST00000650821.1:c.-19-29537_-19-29536del ENSP00000498246.1:n.-19-29537_-19-29536del
ENST00000515655.5:c.-19-29537_-19-29536del ENSP00000426917.1:n.-19-29537_-19-29536del
NM_001257386.1:c.-19-29537_-19-29536del NP_001244315.1:n.-19-29537_-19-29536del
XM_005263355.2:c.-19-29537_-19-29536del XP_005263412.1:n.-19-29537_-19-29536del
XM_011532420.1:c.-19-29537_-19-29536del XP_011530722.1:n.-19-29537_-19-29536del
NM_001257386.2:c.-19-29537_-19-29536del NP_001244315.1:n.-19-29537_-19-29536del
NM_001348985.1:c.-19-29537_-19-29536del NP_001335914.1:n.-19-29537_-19-29536del
XM_005263355.4:c.-19-29537_-19-29536del XP_005263412.1:n.-19-29537_-19-29536del
XM_011532420.3:c.-19-29537_-19-29536del XP_011530722.1:n.-19-29537_-19-29536del