Canonical Allele Identifier: CA100899906
Gene: ABCG2 HGNC NCBI

Linked Data

dbSNP Id: rs760888046

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88169594G>A , CM000666.2:g.88169594G>A GRCh38
NC_000004.11:g.89090746G>A , CM000666.1:g.89090746G>A GRCh37
NC_000004.10:g.89309770G>A NCBI36
NG_032067.2:g.66729C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000650821.1:c.-19-29580C>T ENSP00000498246.1:n.-19-29580C>T
ENST00000515655.5:c.-19-29580C>T ENSP00000426917.1:n.-19-29580C>T
NM_001257386.1:c.-19-29580C>T NP_001244315.1:n.-19-29580C>T
XM_005263355.2:c.-19-29580C>T XP_005263412.1:n.-19-29580C>T
XM_011532420.1:c.-19-29580C>T XP_011530722.1:n.-19-29580C>T
NM_001257386.2:c.-19-29580C>T NP_001244315.1:n.-19-29580C>T
NM_001348985.1:c.-19-29580C>T NP_001335914.1:n.-19-29580C>T
XM_005263355.4:c.-19-29580C>T XP_005263412.1:n.-19-29580C>T
XM_011532420.3:c.-19-29580C>T XP_011530722.1:n.-19-29580C>T