Canonical Allele Identifier: CA1474633716
Gene: ABCG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88169590T= , CM000666.2:g.88169590T= GRCh38
NC_000004.11:g.89090742T= , CM000666.1:g.89090742T= GRCh37
NC_000004.10:g.89309766T= NCBI36
NG_032067.2:g.66733A=

Transcript Alleles

HGVS Amino-acid change
ENST00000650821.1:c.-19-29576A= ENSP00000498246.1:n.-19-29576A=
ENST00000515655.5:c.-19-29576A= ENSP00000426917.1:n.-19-29576A=
NM_001257386.1:c.-19-29576A= NP_001244315.1:n.-19-29576A=
XM_005263355.2:c.-19-29576A= XP_005263412.1:n.-19-29576A=
XM_011532420.1:c.-19-29576A= XP_011530722.1:n.-19-29576A=
NM_001257386.2:c.-19-29576A= NP_001244315.1:n.-19-29576A=
NM_001348985.1:c.-19-29576A= NP_001335914.1:n.-19-29576A=
XM_005263355.4:c.-19-29576A= XP_005263412.1:n.-19-29576A=
XM_011532420.3:c.-19-29576A= XP_011530722.1:n.-19-29576A=