Canonical Allele Identifier: CA1474616624
Gene: ABCG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88131086C= , CM000666.2:g.88131086C= GRCh38
NC_000004.11:g.89052238C= , CM000666.1:g.89052238C= GRCh37
NC_000004.10:g.89271262C= NCBI36
NG_032067.2:g.105237G=

Transcript Alleles

HGVS Amino-acid change
ENST00000237612.8:c.506G= MANE Select ENSP00000237612.3:p.Gly169=
ENST00000650821.1:c.506G= ENSP00000498246.1:p.Gly169=
ENST00000237612.7:c.506G= ENSP00000237612.3:p.Gly169=
ENST00000515655.5:c.506G= ENSP00000426917.1:p.Gly169=
NM_001257386.1:c.506G= NP_001244315.1:p.Gly169=
NM_004827.2:c.506G= NP_004818.2:p.Gly169=
XM_005263354.2:c.506G= XP_005263411.1:p.Gly169=
XM_005263355.2:c.506G= XP_005263412.1:p.Gly169=
XM_005263356.2:c.506G= XP_005263413.1:p.Gly169=
XM_011532420.1:c.506G= XP_011530722.1:p.Gly169=
NM_001257386.2:c.506G= NP_001244315.1:p.Gly169=
NM_001348985.1:c.506G= NP_001335914.1:p.Gly169=
NM_001348986.1:c.506G= NP_001335915.1:p.Gly169=
NM_001348987.1:c.506G= NP_001335916.1:p.Gly169=
NM_001348988.1:c.506G= NP_001335917.1:p.Gly169=
NM_001348989.1:c.506G= NP_001335918.1:p.Gly169=
XM_005263355.4:c.506G= XP_005263412.1:p.Gly169=
XM_011532420.3:c.506G= XP_011530722.1:p.Gly169=
XM_017008852.2:c.506G= XP_016864341.1:p.Gly169=
NM_004827.3:c.506G= MANE Select NP_004818.2:p.Gly169=
NM_001348989.2:c.506G= NP_001335918.1:p.Gly169=