Canonical Allele Identifier: CA1065137932

Gene: ABCG2

Linked Data

• dbSNP Id: rs1727680540

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88169720T>C , CM000666.2:g.88169720T>C	GRCh38
NC_000004.11:g.89090872T>C , CM000666.1:g.89090872T>C	GRCh37
NC_000004.10:g.89309896T>C	NCBI36
NG_032067.2:g.66603A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650821.1:c.-19-29706A>G	ENSP00000498246.1:n.-19-29706A>G
ENST00000515655.5:c.-19-29706A>G	ENSP00000426917.1:n.-19-29706A>G
NM_001257386.1:c.-19-29706A>G	NP_001244315.1:n.-19-29706A>G
XM_005263355.2:c.-19-29706A>G	XP_005263412.1:n.-19-29706A>G
XM_011532420.1:c.-19-29706A>G	XP_011530722.1:n.-19-29706A>G
NM_001257386.2:c.-19-29706A>G	NP_001244315.1:n.-19-29706A>G
NM_001348985.1:c.-19-29706A>G	NP_001335914.1:n.-19-29706A>G
XM_005263355.4:c.-19-29706A>G	XP_005263412.1:n.-19-29706A>G
XM_011532420.3:c.-19-29706A>G	XP_011530722.1:n.-19-29706A>G