Canonical Allele Identifier: CA552875579

Gene: ABCG2

Linked Data

• dbSNP Id: rs1468400299
• gnomAD v2: 4-89090940-AG-A
• gnomAD v3: 4-88169788-AG-A
• gnomAD v4: 4-88169788-AG-A
• MyVariant Identifiers: chr4:g.89090941del (hg19) ; chr4:g.88169789del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88169790del , CM000666.2:g.88169790del	GRCh38
NC_000004.11:g.89090942del , CM000666.1:g.89090942del	GRCh37
NC_000004.10:g.89309966del	NCBI36
NG_032067.2:g.66534del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650821.1:c.-19-29775del	ENSP00000498246.1:n.-19-29775del
ENST00000515655.5:c.-19-29775del	ENSP00000426917.1:n.-19-29775del
NM_001257386.1:c.-19-29775del	NP_001244315.1:n.-19-29775del
XM_005263355.2:c.-19-29775del	XP_005263412.1:n.-19-29775del
XM_011532420.1:c.-19-29775del	XP_011530722.1:n.-19-29775del
NM_001257386.2:c.-19-29775del	NP_001244315.1:n.-19-29775del
NM_001348985.1:c.-19-29775del	NP_001335914.1:n.-19-29775del
XM_005263355.4:c.-19-29775del	XP_005263412.1:n.-19-29775del
XM_011532420.3:c.-19-29775del	XP_011530722.1:n.-19-29775del