Canonical Allele Identifier: CA1474633684
Gene: ABCG2 HGNC NCBI

Linked Data

dbSNP Id: rs1727673471

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88169539T>C , CM000666.2:g.88169539T>C GRCh38
NC_000004.11:g.89090691T>C , CM000666.1:g.89090691T>C GRCh37
NC_000004.10:g.89309715T>C NCBI36
NG_032067.2:g.66784A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000650821.1:c.-19-29525A>G ENSP00000498246.1:n.-19-29525A>G
ENST00000515655.5:c.-19-29525A>G ENSP00000426917.1:n.-19-29525A>G
NM_001257386.1:c.-19-29525A>G NP_001244315.1:n.-19-29525A>G
XM_005263355.2:c.-19-29525A>G XP_005263412.1:n.-19-29525A>G
XM_011532420.1:c.-19-29525A>G XP_011530722.1:n.-19-29525A>G
NM_001257386.2:c.-19-29525A>G NP_001244315.1:n.-19-29525A>G
NM_001348985.1:c.-19-29525A>G NP_001335914.1:n.-19-29525A>G
XM_005263355.4:c.-19-29525A>G XP_005263412.1:n.-19-29525A>G
XM_011532420.3:c.-19-29525A>G XP_011530722.1:n.-19-29525A>G