Canonical Allele Identifier: CA100899932
Gene: ABCG2 HGNC NCBI

Linked Data

dbSNP Id: rs887363017
MyVariant Identifiers: chr4:g.89090858A>T (hg19) chr4:g.88169706A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88169706A>T , CM000666.2:g.88169706A>T GRCh38
NC_000004.11:g.89090858A>T , CM000666.1:g.89090858A>T GRCh37
NC_000004.10:g.89309882A>T NCBI36
NG_032067.2:g.66617T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000650821.1:c.-19-29692T>A ENSP00000498246.1:n.-19-29692T>A
ENST00000515655.5:c.-19-29692T>A ENSP00000426917.1:n.-19-29692T>A
NM_001257386.1:c.-19-29692T>A NP_001244315.1:n.-19-29692T>A
XM_005263355.2:c.-19-29692T>A XP_005263412.1:n.-19-29692T>A
XM_011532420.1:c.-19-29692T>A XP_011530722.1:n.-19-29692T>A
NM_001257386.2:c.-19-29692T>A NP_001244315.1:n.-19-29692T>A
NM_001348985.1:c.-19-29692T>A NP_001335914.1:n.-19-29692T>A
XM_005263355.4:c.-19-29692T>A XP_005263412.1:n.-19-29692T>A
XM_011532420.3:c.-19-29692T>A XP_011530722.1:n.-19-29692T>A
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