Canonical Allele Identifier: CA1474633755
Gene: ABCG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88169701T= , CM000666.2:g.88169701T= GRCh38
NC_000004.11:g.89090853T= , CM000666.1:g.89090853T= GRCh37
NC_000004.10:g.89309877T= NCBI36
NG_032067.2:g.66622A=

Transcript Alleles

HGVS Amino-acid change
ENST00000650821.1:c.-19-29687A= ENSP00000498246.1:n.-19-29687A=
ENST00000515655.5:c.-19-29687A= ENSP00000426917.1:n.-19-29687A=
NM_001257386.1:c.-19-29687A= NP_001244315.1:n.-19-29687A=
XM_005263355.2:c.-19-29687A= XP_005263412.1:n.-19-29687A=
XM_011532420.1:c.-19-29687A= XP_011530722.1:n.-19-29687A=
NM_001257386.2:c.-19-29687A= NP_001244315.1:n.-19-29687A=
NM_001348985.1:c.-19-29687A= NP_001335914.1:n.-19-29687A=
XM_005263355.4:c.-19-29687A= XP_005263412.1:n.-19-29687A=
XM_011532420.3:c.-19-29687A= XP_011530722.1:n.-19-29687A=