Canonical Allele Identifier: CA100889247
Gene: ABCG2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1481012

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88117930A>G , CM000666.2:g.88117930A>G GRCh38
NC_000004.11:g.89039082A>G , CM000666.1:g.89039082A>G GRCh37
NC_000004.10:g.89258106A>G NCBI36
NG_032067.2:g.118393T>C

Transcript Alleles

HGVS Amino-acid change
NM_001257386.1:c.841+179T>C VV NP_001244315.1:p.=
NM_004827.2:c.841+179T>C VV NP_004818.2:p.=
XM_005263354.2:c.841+179T>C XP_005263411.1:p.=
XM_005263355.2:c.841+179T>C XP_005263412.1:p.=
XM_005263356.2:c.841+179T>C XP_005263413.1:p.=
XM_011532420.1:c.841+179T>C XP_011530722.1:p.=
NM_001257386.2:c.841+179T>C VV NP_001244315.1:p.=
NM_001348985.1:c.841+179T>C VV NP_001335914.1:p.=
NM_001348986.1:c.841+179T>C VV NP_001335915.1:p.=
NM_001348987.1:c.841+179T>C VV NP_001335916.1:p.=
NM_001348988.1:c.841+179T>C VV NP_001335917.1:p.=
NM_001348989.1:c.841+179T>C VV NP_001335918.1:p.=
XM_005263355.4:c.841+179T>C XP_005263412.1:p.=
XM_011532420.3:c.841+179T>C XP_011530722.1:p.=
XM_017008852.2:c.841+179T>C XP_016864341.1:p.=
NM_004827.3:c.841+179T>C VV MANE Preferred NP_004818.2:p.=
ENST00000237612.7:c.841+179T>C ENSP00000237612.3:p.=
ENST00000515655.5:c.841+179T>C ENSP00000426917.1:p.=