Canonical Allele Identifier: CA100899900

Gene: ABCG2

Linked Data

• dbSNP Id: rs929333735
• gnomAD v3: 4-88169570-T-G
• gnomAD v4: 4-88169570-T-G
• MyVariant Identifiers: chr4:g.89090722T>G (hg19) ; chr4:g.88169570T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88169570T>G , CM000666.2:g.88169570T>G	GRCh38
NC_000004.11:g.89090722T>G , CM000666.1:g.89090722T>G	GRCh37
NC_000004.10:g.89309746T>G	NCBI36
NG_032067.2:g.66753A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650821.1:c.-19-29556A>C	ENSP00000498246.1:n.-19-29556A>C
ENST00000515655.5:c.-19-29556A>C	ENSP00000426917.1:n.-19-29556A>C
NM_001257386.1:c.-19-29556A>C	NP_001244315.1:n.-19-29556A>C
XM_005263355.2:c.-19-29556A>C	XP_005263412.1:n.-19-29556A>C
XM_011532420.1:c.-19-29556A>C	XP_011530722.1:n.-19-29556A>C
NM_001257386.2:c.-19-29556A>C	NP_001244315.1:n.-19-29556A>C
NM_001348985.1:c.-19-29556A>C	NP_001335914.1:n.-19-29556A>C
XM_005263355.4:c.-19-29556A>C	XP_005263412.1:n.-19-29556A>C
XM_011532420.3:c.-19-29556A>C	XP_011530722.1:n.-19-29556A>C