Canonical Allele Identifier: CA1474633797
Gene: ABCG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88169785A= , CM000666.2:g.88169785A= GRCh38
NC_000004.11:g.89090937A= , CM000666.1:g.89090937A= GRCh37
NC_000004.10:g.89309961A= NCBI36
NG_032067.2:g.66538T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650821.1:c.-19-29771T= ENSP00000498246.1:n.-19-29771T=
ENST00000515655.5:c.-19-29771T= ENSP00000426917.1:n.-19-29771T=
NM_001257386.1:c.-19-29771T= NP_001244315.1:n.-19-29771T=
XM_005263355.2:c.-19-29771T= XP_005263412.1:n.-19-29771T=
XM_011532420.1:c.-19-29771T= XP_011530722.1:n.-19-29771T=
NM_001257386.2:c.-19-29771T= NP_001244315.1:n.-19-29771T=
NM_001348985.1:c.-19-29771T= NP_001335914.1:n.-19-29771T=
XM_005263355.4:c.-19-29771T= XP_005263412.1:n.-19-29771T=
XM_011532420.3:c.-19-29771T= XP_011530722.1:n.-19-29771T=