Canonical Allele Identifier: CA11784012
Gene: ABCG2 HGNC NCBI

Linked Data

dbSNP Id: rs17731799

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88147303G>T , CM000666.2:g.88147303G>T GRCh38
NC_000004.11:g.89068455G>T , CM000666.1:g.89068455G>T GRCh37
NC_000004.10:g.89287479G>T NCBI36
NG_032067.2:g.89020C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000237612.8:c.-19-7289C>A MANE Select ENSP00000237612.3:p.=
ENST00000503830.2:c.-19-7289C>A ENSP00000426934.2:p.=
ENST00000505480.6:c.-19-7289C>A ENSP00000426916.2:p.=
ENST00000650821.1:c.-19-7289C>A ENSP00000498246.1:p.=
ENST00000237612.7:c.-19-7289C>A ENSP00000237612.3:p.=
ENST00000503830.1:n.36-7289C>A ENSP00000426934.1:p.=
ENST00000505480.5:n.96-7289C>A ENSP00000426916.1:p.=
ENST00000515655.5:c.-19-7289C>A ENSP00000426917.1:p.=
NM_001257386.1:c.-19-7289C>A NP_001244315.1:p.=
NM_004827.2:c.-19-7289C>A NP_004818.2:p.=
XM_005263354.2:c.-19-7289C>A XP_005263411.1:p.=
XM_005263355.2:c.-19-7289C>A XP_005263412.1:p.=
XM_005263356.2:c.-19-7289C>A XP_005263413.1:p.=
XM_011532420.1:c.-19-7289C>A XP_011530722.1:p.=
NM_001257386.2:c.-19-7289C>A NP_001244315.1:p.=
NM_001348985.1:c.-19-7289C>A NP_001335914.1:p.=
NM_001348986.1:c.-19-7289C>A NP_001335915.1:p.=
NM_001348987.1:c.-19-7289C>A NP_001335916.1:p.=
NM_001348988.1:c.-20+2889C>A NP_001335917.1:p.=
NM_001348989.1:c.-19-7289C>A NP_001335918.1:p.=
XM_005263355.4:c.-19-7289C>A XP_005263412.1:p.=
XM_011532420.3:c.-19-7289C>A XP_011530722.1:p.=
XM_017008852.2:c.-19-7289C>A XP_016864341.1:p.=
NM_004827.3:c.-19-7289C>A MANE Select NP_004818.2:p.=
NM_001348989.2:c.-19-7289C>A NP_001335918.1:p.=