Canonical Allele Identifier: CA357630228

Gene: ABCG2

Linked Data

• dbSNP Id: rs1724829467
• gnomAD v4: 4-88131072-C-T
• MyVariant Identifiers: chr4:g.89052224C>T (hg19) ; chr4:g.88131072C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88131072C>T , CM000666.2:g.88131072C>T	GRCh38
NC_000004.11:g.89052224C>T , CM000666.1:g.89052224C>T	GRCh37
NC_000004.10:g.89271248C>T	NCBI36
NG_032067.2:g.105251G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000237612.8:c.520G>A MANE Select	ENSP00000237612.3:p.Ala174Thr
ENST00000650821.1:c.520G>A	ENSP00000498246.1:p.Ala174Thr
ENST00000237612.7:c.520G>A	ENSP00000237612.3:p.Ala174Thr
ENST00000515655.5:c.520G>A	ENSP00000426917.1:p.Ala174Thr
NM_001257386.1:c.520G>A	NP_001244315.1:p.Ala174Thr
NM_004827.2:c.520G>A	NP_004818.2:p.Ala174Thr
XM_005263354.2:c.520G>A	XP_005263411.1:p.Ala174Thr
XM_005263355.2:c.520G>A	XP_005263412.1:p.Ala174Thr
XM_005263356.2:c.520G>A	XP_005263413.1:p.Ala174Thr
XM_011532420.1:c.520G>A	XP_011530722.1:p.Ala174Thr
NM_001257386.2:c.520G>A	NP_001244315.1:p.Ala174Thr
NM_001348985.1:c.520G>A	NP_001335914.1:p.Ala174Thr
NM_001348986.1:c.520G>A	NP_001335915.1:p.Ala174Thr
NM_001348987.1:c.520G>A	NP_001335916.1:p.Ala174Thr
NM_001348988.1:c.520G>A	NP_001335917.1:p.Ala174Thr
NM_001348989.1:c.520G>A	NP_001335918.1:p.Ala174Thr
XM_005263355.4:c.520G>A	XP_005263412.1:p.Ala174Thr
XM_011532420.3:c.520G>A	XP_011530722.1:p.Ala174Thr
XM_017008852.2:c.520G>A	XP_016864341.1:p.Ala174Thr
NM_004827.3:c.520G>A MANE Select	NP_004818.2:p.Ala174Thr
NM_001348989.2:c.520G>A	NP_001335918.1:p.Ala174Thr