Canonical Allele Identifier: CA799633445

Gene: ABCG2

Linked Data

• dbSNP Id: rs1231508888
• MyVariant Identifiers: chr4:g.89090901C>G (hg19) ; chr4:g.88169749C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88169749C>G , CM000666.2:g.88169749C>G	GRCh38
NC_000004.11:g.89090901C>G , CM000666.1:g.89090901C>G	GRCh37
NC_000004.10:g.89309925C>G	NCBI36
NG_032067.2:g.66574G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000650821.1:c.-19-29735G>C	ENSP00000498246.1:n.-19-29735G>C
ENST00000515655.5:c.-19-29735G>C	ENSP00000426917.1:n.-19-29735G>C
NM_001257386.1:c.-19-29735G>C	NP_001244315.1:n.-19-29735G>C
XM_005263355.2:c.-19-29735G>C	XP_005263412.1:n.-19-29735G>C
XM_011532420.1:c.-19-29735G>C	XP_011530722.1:n.-19-29735G>C
NM_001257386.2:c.-19-29735G>C	NP_001244315.1:n.-19-29735G>C
NM_001348985.1:c.-19-29735G>C	NP_001335914.1:n.-19-29735G>C
XM_005263355.4:c.-19-29735G>C	XP_005263412.1:n.-19-29735G>C
XM_011532420.3:c.-19-29735G>C	XP_011530722.1:n.-19-29735G>C