Canonical Allele Identifier: CA346670370
Gene: ABCG8 HGNC NCBI

Linked Data

dbSNP Id: rs1413219813
gnomAD v2: 2-44102369-C-A
gnomAD v3: 2-43875230-C-A
gnomAD v4: 2-43875230-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43875230C>A , CM000664.2:g.43875230C>A GRCh38
NC_000002.11:g.44102369C>A , CM000664.1:g.44102369C>A GRCh37
NC_000002.10:g.43955873C>A NCBI36
NG_008884.1:g.41267C>A
NG_008884.2:g.48289C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000272286.4:c.1573C>A MANE Select ENSP00000272286.2:p.Leu525Ile
ENST00000272286.2:c.1573C>A ENSP00000272286.2:p.Leu525Ile
NM_022437.2:c.1573C>A NP_071882.1:p.Leu525Ile
XM_005264483.2:c.1570C>A XP_005264540.1:p.Leu524Ile
XM_011533029.1:c.1585C>A XP_011531331.1:p.Leu529Ile
XM_011533030.1:c.1582C>A XP_011531332.1:p.Leu528Ile
XM_011533031.1:c.1357C>A XP_011531333.1:p.Leu453Ile
XR_939707.1:n.2075C>A
NM_001357321.1:c.1570C>A NP_001344250.1:p.Leu524Ile
XM_011533029.2:c.1585C>A XP_011531331.1:p.Leu529Ile
XM_011533030.2:c.1582C>A XP_011531332.1:p.Leu528Ile
XR_001738891.1:n.2089C>A
XR_939707.2:n.2089C>A
NM_022437.3:c.1573C>A MANE Select NP_071882.1:p.Leu525Ile
NM_001357321.2:c.1570C>A NP_001344250.1:p.Leu524Ile