Canonical Allele Identifier: CA1065137860
Gene: ABCG2 HGNC NCBI

Linked Data

dbSNP Id: rs1727673201
gnomAD v3: 4-88169532-C-A
gnomAD v4: 4-88169532-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88169532C>A , CM000666.2:g.88169532C>A GRCh38
NC_000004.11:g.89090684C>A , CM000666.1:g.89090684C>A GRCh37
NC_000004.10:g.89309708C>A NCBI36
NG_032067.2:g.66791G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000650821.1:c.-19-29518G>T ENSP00000498246.1:n.-19-29518G>T
ENST00000515655.5:c.-19-29518G>T ENSP00000426917.1:n.-19-29518G>T
NM_001257386.1:c.-19-29518G>T NP_001244315.1:n.-19-29518G>T
XM_005263355.2:c.-19-29518G>T XP_005263412.1:n.-19-29518G>T
XM_011532420.1:c.-19-29518G>T XP_011530722.1:n.-19-29518G>T
NM_001257386.2:c.-19-29518G>T NP_001244315.1:n.-19-29518G>T
NM_001348985.1:c.-19-29518G>T NP_001335914.1:n.-19-29518G>T
XM_005263355.4:c.-19-29518G>T XP_005263412.1:n.-19-29518G>T
XM_011532420.3:c.-19-29518G>T XP_011530722.1:n.-19-29518G>T