Canonical Allele Identifier: CA1065137914
Gene: ABCG2 HGNC NCBI

Linked Data

dbSNP Id: rs1727679611
gnomAD v3: 4-88169704-G-T
gnomAD v4: 4-88169704-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88169704G>T , CM000666.2:g.88169704G>T GRCh38
NC_000004.11:g.89090856G>T , CM000666.1:g.89090856G>T GRCh37
NC_000004.10:g.89309880G>T NCBI36
NG_032067.2:g.66619C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000650821.1:c.-19-29690C>A ENSP00000498246.1:n.-19-29690C>A
ENST00000515655.5:c.-19-29690C>A ENSP00000426917.1:n.-19-29690C>A
NM_001257386.1:c.-19-29690C>A NP_001244315.1:n.-19-29690C>A
XM_005263355.2:c.-19-29690C>A XP_005263412.1:n.-19-29690C>A
XM_011532420.1:c.-19-29690C>A XP_011530722.1:n.-19-29690C>A
NM_001257386.2:c.-19-29690C>A NP_001244315.1:n.-19-29690C>A
NM_001348985.1:c.-19-29690C>A NP_001335914.1:n.-19-29690C>A
XM_005263355.4:c.-19-29690C>A XP_005263412.1:n.-19-29690C>A
XM_011532420.3:c.-19-29690C>A XP_011530722.1:n.-19-29690C>A
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