Canonical Allele Identifier: CA1474633681
Gene: ABCG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88169533C= , CM000666.2:g.88169533C= GRCh38
NC_000004.11:g.89090685C= , CM000666.1:g.89090685C= GRCh37
NC_000004.10:g.89309709C= NCBI36
NG_032067.2:g.66790G=

Transcript Alleles

HGVS Amino-acid change
ENST00000650821.1:c.-19-29519G= ENSP00000498246.1:n.-19-29519G=
ENST00000515655.5:c.-19-29519G= ENSP00000426917.1:n.-19-29519G=
NM_001257386.1:c.-19-29519G= NP_001244315.1:n.-19-29519G=
XM_005263355.2:c.-19-29519G= XP_005263412.1:n.-19-29519G=
XM_011532420.1:c.-19-29519G= XP_011530722.1:n.-19-29519G=
NM_001257386.2:c.-19-29519G= NP_001244315.1:n.-19-29519G=
NM_001348985.1:c.-19-29519G= NP_001335914.1:n.-19-29519G=
XM_005263355.4:c.-19-29519G= XP_005263412.1:n.-19-29519G=
XM_011532420.3:c.-19-29519G= XP_011530722.1:n.-19-29519G=