Canonical Allele Identifier: CA46434993
Gene: ABCG8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1221022
ClinVar RCV Id: RCV001595584
dbSNP Id: rs41360247

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43846517T>C , CM000664.2:g.43846517T>C GRCh38
NC_000002.11:g.44073656T>C , CM000664.1:g.44073656T>C GRCh37
NC_000002.10:g.43927160T>C NCBI36
NG_008884.1:g.12554T>C
NG_008884.2:g.19576T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000272286.4:c.322+206T>C MANE Select ENSP00000272286.2:p.=
ENST00000643284.1:n.985T>C
ENST00000644611.1:c.334+206T>C ENSP00000495423.1:p.=
ENST00000272286.2:c.322+206T>C ENSP00000272286.2:p.=
NM_022437.2:c.322+206T>C NP_071882.1:p.=
XM_005264483.2:c.322+206T>C XP_005264540.1:p.=
XM_011533029.1:c.334+206T>C XP_011531331.1:p.=
XM_011533030.1:c.334+206T>C XP_011531332.1:p.=
XM_011533031.1:c.106+206T>C XP_011531333.1:p.=
XR_939707.1:n.824+206T>C
NM_001357321.1:c.322+206T>C NP_001344250.1:p.=
XM_011533029.2:c.334+206T>C XP_011531331.1:p.=
XM_011533030.2:c.334+206T>C XP_011531332.1:p.=
XR_001738891.1:n.838+206T>C
XR_939707.2:n.838+206T>C
NM_022437.3:c.322+206T>C MANE Select NP_071882.1:p.=
NM_001357321.2:c.322+206T>C NP_001344250.1:p.=