Canonical Allele Identifier: CA1065137873
Gene: ABCG2 HGNC NCBI

Linked Data

dbSNP Id: rs1727674204
gnomAD v3: 4-88169552-A-G
gnomAD v4: 4-88169552-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88169552A>G , CM000666.2:g.88169552A>G GRCh38
NC_000004.11:g.89090704A>G , CM000666.1:g.89090704A>G GRCh37
NC_000004.10:g.89309728A>G NCBI36
NG_032067.2:g.66771T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000650821.1:c.-19-29538T>C ENSP00000498246.1:n.-19-29538T>C
ENST00000515655.5:c.-19-29538T>C ENSP00000426917.1:n.-19-29538T>C
NM_001257386.1:c.-19-29538T>C NP_001244315.1:n.-19-29538T>C
XM_005263355.2:c.-19-29538T>C XP_005263412.1:n.-19-29538T>C
XM_011532420.1:c.-19-29538T>C XP_011530722.1:n.-19-29538T>C
NM_001257386.2:c.-19-29538T>C NP_001244315.1:n.-19-29538T>C
NM_001348985.1:c.-19-29538T>C NP_001335914.1:n.-19-29538T>C
XM_005263355.4:c.-19-29538T>C XP_005263412.1:n.-19-29538T>C
XM_011532420.3:c.-19-29538T>C XP_011530722.1:n.-19-29538T>C