Canonical Allele Identifier: CA1636957
Gene: ABCG8 HGNC NCBI

Linked Data

dbSNP Id: rs760729319
gnomAD v2: 2-44073409-A-G
gnomAD v3: 2-43846270-A-G
gnomAD v4: 2-43846270-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43846270A>G , CM000664.2:g.43846270A>G GRCh38
NC_000002.11:g.44073409A>G , CM000664.1:g.44073409A>G GRCh37
NC_000002.10:g.43926913A>G NCBI36
NG_008884.1:g.12307A>G
NG_008884.2:g.19329A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000272286.4:c.281A>G MANE Select ENSP00000272286.2:p.Lys94Arg
ENST00000643284.1:n.738A>G
ENST00000644611.1:c.293A>G ENSP00000495423.1:p.Lys98Arg
ENST00000272286.2:c.281A>G ENSP00000272286.2:p.Lys94Arg
NM_022437.2:c.281A>G NP_071882.1:p.Lys94Arg
XM_005264483.2:c.281A>G XP_005264540.1:p.Lys94Arg
XM_011533029.1:c.293A>G XP_011531331.1:p.Lys98Arg
XM_011533030.1:c.293A>G XP_011531332.1:p.Lys98Arg
XM_011533031.1:c.65A>G XP_011531333.1:p.Lys22Arg
XR_939707.1:n.783A>G
NM_001357321.1:c.281A>G NP_001344250.1:p.Lys94Arg
XM_011533029.2:c.293A>G XP_011531331.1:p.Lys98Arg
XM_011533030.2:c.293A>G XP_011531332.1:p.Lys98Arg
XR_001738891.1:n.797A>G
XR_939707.2:n.797A>G
NM_022437.3:c.281A>G MANE Select NP_071882.1:p.Lys94Arg
NM_001357321.2:c.281A>G NP_001344250.1:p.Lys94Arg