Canonical Allele Identifier: CA46470493
Gene: ABCG8 HGNC NCBI

Linked Data

dbSNP Id: rs532221631
gnomAD v3: 2-43875017-C-G
gnomAD v4: 2-43875017-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43875017C>G , CM000664.2:g.43875017C>G GRCh38
NC_000002.11:g.44102156C>G , CM000664.1:g.44102156C>G GRCh37
NC_000002.10:g.43955660C>G NCBI36
NG_008884.1:g.41054C>G
NG_008884.2:g.48076C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000272286.4:c.1489-129C>G MANE Select ENSP00000272286.2:n.1489-129C>G
ENST00000272286.2:c.1489-129C>G ENSP00000272286.2:n.1489-129C>G
NM_022437.2:c.1489-129C>G NP_071882.1:n.1489-129C>G
XM_005264483.2:c.1486-129C>G XP_005264540.1:n.1486-129C>G
XM_011533029.1:c.1501-129C>G XP_011531331.1:n.1501-129C>G
XM_011533030.1:c.1498-129C>G XP_011531332.1:n.1498-129C>G
XM_011533031.1:c.1273-129C>G XP_011531333.1:n.1273-129C>G
XR_939707.1:n.1991-129C>G
NM_001357321.1:c.1486-129C>G NP_001344250.1:n.1486-129C>G
XM_011533029.2:c.1501-129C>G XP_011531331.1:n.1501-129C>G
XM_011533030.2:c.1498-129C>G XP_011531332.1:n.1498-129C>G
XR_001738891.1:n.2005-129C>G
XR_939707.2:n.2005-129C>G
NM_022437.3:c.1489-129C>G MANE Select NP_071882.1:n.1489-129C>G
NM_001357321.2:c.1486-129C>G NP_001344250.1:n.1486-129C>G