Canonical Allele Identifier: CA100899951

Gene: ABCG2

Linked Data

• dbSNP Id: rs1010991819
• MyVariant Identifiers: chr4:g.89090940A>G (hg19) ; chr4:g.88169788A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88169788A>G , CM000666.2:g.88169788A>G	GRCh38
NC_000004.11:g.89090940A>G , CM000666.1:g.89090940A>G	GRCh37
NC_000004.10:g.89309964A>G	NCBI36
NG_032067.2:g.66535T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000650821.1:c.-19-29774T>C	ENSP00000498246.1:n.-19-29774T>C
ENST00000515655.5:c.-19-29774T>C	ENSP00000426917.1:n.-19-29774T>C
NM_001257386.1:c.-19-29774T>C	NP_001244315.1:n.-19-29774T>C
XM_005263355.2:c.-19-29774T>C	XP_005263412.1:n.-19-29774T>C
XM_011532420.1:c.-19-29774T>C	XP_011530722.1:n.-19-29774T>C
NM_001257386.2:c.-19-29774T>C	NP_001244315.1:n.-19-29774T>C
NM_001348985.1:c.-19-29774T>C	NP_001335914.1:n.-19-29774T>C
XM_005263355.4:c.-19-29774T>C	XP_005263412.1:n.-19-29774T>C
XM_011532420.3:c.-19-29774T>C	XP_011530722.1:n.-19-29774T>C