Canonical Allele Identifier: CA532282381
Gene: ABCG8 HGNC NCBI

Linked Data

dbSNP Id: rs1430910559
gnomAD v2: 2-44073717-T-G
gnomAD v3: 2-43846578-T-G
gnomAD v4: 2-43846578-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43846578T>G , CM000664.2:g.43846578T>G GRCh38
NC_000002.11:g.44073717T>G , CM000664.1:g.44073717T>G GRCh37
NC_000002.10:g.43927221T>G NCBI36
NG_008884.1:g.12615T>G
NG_008884.2:g.19637T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000272286.4:c.322+267T>G MANE Select ENSP00000272286.2:n.322+267T>G
ENST00000643284.1:n.1046T>G
ENST00000644611.1:c.334+267T>G ENSP00000495423.1:n.334+267T>G
ENST00000272286.2:c.322+267T>G ENSP00000272286.2:n.322+267T>G
NM_022437.2:c.322+267T>G NP_071882.1:n.322+267T>G
XM_005264483.2:c.322+267T>G XP_005264540.1:n.322+267T>G
XM_011533029.1:c.334+267T>G XP_011531331.1:n.334+267T>G
XM_011533030.1:c.334+267T>G XP_011531332.1:n.334+267T>G
XM_011533031.1:c.106+267T>G XP_011531333.1:n.106+267T>G
XR_939707.1:n.824+267T>G
NM_001357321.1:c.322+267T>G NP_001344250.1:n.322+267T>G
XM_011533029.2:c.334+267T>G XP_011531331.1:n.334+267T>G
XM_011533030.2:c.334+267T>G XP_011531332.1:n.334+267T>G
XR_001738891.1:n.838+267T>G
XR_939707.2:n.838+267T>G
NM_022437.3:c.322+267T>G MANE Select NP_071882.1:n.322+267T>G
NM_001357321.2:c.322+267T>G NP_001344250.1:n.322+267T>G