Canonical Allele Identifier: CA100899956

Gene: ABCG2

Linked Data

• dbSNP Id: rs555788356
• gnomAD v3: 4-88169807-A-C
• gnomAD v4: 4-88169807-A-C
• MyVariant Identifiers: chr4:g.89090959A>C (hg19) ; chr4:g.88169807A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88169807A>C , CM000666.2:g.88169807A>C	GRCh38
NC_000004.11:g.89090959A>C , CM000666.1:g.89090959A>C	GRCh37
NC_000004.10:g.89309983A>C	NCBI36
NG_032067.2:g.66516T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650821.1:c.-19-29793T>G	ENSP00000498246.1:n.-19-29793T>G
ENST00000515655.5:c.-19-29793T>G	ENSP00000426917.1:n.-19-29793T>G
NM_001257386.1:c.-19-29793T>G	NP_001244315.1:n.-19-29793T>G
XM_005263355.2:c.-19-29793T>G	XP_005263412.1:n.-19-29793T>G
XM_011532420.1:c.-19-29793T>G	XP_011530722.1:n.-19-29793T>G
NM_001257386.2:c.-19-29793T>G	NP_001244315.1:n.-19-29793T>G
NM_001348985.1:c.-19-29793T>G	NP_001335914.1:n.-19-29793T>G
XM_005263355.4:c.-19-29793T>G	XP_005263412.1:n.-19-29793T>G
XM_011532420.3:c.-19-29793T>G	XP_011530722.1:n.-19-29793T>G