Canonical Allele Identifier: CA3004923

Gene: ABCG2

Linked Data

• dbSNP Id: rs748501399
• ExAC: 4:89052334 C / T
• gnomAD v2: 4-89052334-C-T
• gnomAD v3: 4-88131182-C-T
• gnomAD v4: 4-88131182-C-T
• COSMIC: COSM5431280 ; COSM5431281
• MyVariant Identifiers: chr4:g.89052334C>T (hg19) ; chr4:g.88131182C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88131182C>T , CM000666.2:g.88131182C>T	GRCh38
NC_000004.11:g.89052334C>T , CM000666.1:g.89052334C>T	GRCh37
NC_000004.10:g.89271358C>T	NCBI36
NG_032067.2:g.105141G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237612.8:c.410G>A MANE Select	ENSP00000237612.3:p.Arg137Lys
ENST00000650821.1:c.410G>A	ENSP00000498246.1:p.Arg137Lys
ENST00000237612.7:c.410G>A	ENSP00000237612.3:p.Arg137Lys
ENST00000515655.5:c.410G>A	ENSP00000426917.1:p.Arg137Lys
NM_001257386.1:c.410G>A	NP_001244315.1:p.Arg137Lys
NM_004827.2:c.410G>A	NP_004818.2:p.Arg137Lys
XM_005263354.2:c.410G>A	XP_005263411.1:p.Arg137Lys
XM_005263355.2:c.410G>A	XP_005263412.1:p.Arg137Lys
XM_005263356.2:c.410G>A	XP_005263413.1:p.Arg137Lys
XM_011532420.1:c.410G>A	XP_011530722.1:p.Arg137Lys
NM_001257386.2:c.410G>A	NP_001244315.1:p.Arg137Lys
NM_001348985.1:c.410G>A	NP_001335914.1:p.Arg137Lys
NM_001348986.1:c.410G>A	NP_001335915.1:p.Arg137Lys
NM_001348987.1:c.410G>A	NP_001335916.1:p.Arg137Lys
NM_001348988.1:c.410G>A	NP_001335917.1:p.Arg137Lys
NM_001348989.1:c.410G>A	NP_001335918.1:p.Arg137Lys
XM_005263355.4:c.410G>A	XP_005263412.1:p.Arg137Lys
XM_011532420.3:c.410G>A	XP_011530722.1:p.Arg137Lys
XM_017008852.2:c.410G>A	XP_016864341.1:p.Arg137Lys
NM_004827.3:c.410G>A MANE Select	NP_004818.2:p.Arg137Lys
NM_001348989.2:c.410G>A	NP_001335918.1:p.Arg137Lys