Canonical Allele Identifier: CA1637690
Gene: ABCG8 HGNC NCBI

Linked Data

dbSNP Id: rs768950847
gnomAD v2: 2-44104823-A-G
gnomAD v4: 2-43877684-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43877684A>G , CM000664.2:g.43877684A>G GRCh38
NC_000002.11:g.44104823A>G , CM000664.1:g.44104823A>G GRCh37
NC_000002.10:g.43958327A>G NCBI36
NG_008884.1:g.43721A>G
NG_008884.2:g.50743A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000272286.4:c.1880A>G MANE Select ENSP00000272286.2:p.Asp627Gly
ENST00000272286.2:c.1880A>G ENSP00000272286.2:p.Asp627Gly
NM_022437.2:c.1880A>G NP_071882.1:p.Asp627Gly
XM_005264483.2:c.1877A>G XP_005264540.1:p.Asp626Gly
XM_011533029.1:c.1892A>G XP_011531331.1:p.Asp631Gly
XM_011533030.1:c.1889A>G XP_011531332.1:p.Asp630Gly
XM_011533031.1:c.1664A>G XP_011531333.1:p.Asp555Gly
XR_939707.1:n.2382A>G
NM_001357321.1:c.1877A>G NP_001344250.1:p.Asp626Gly
XM_011533029.2:c.1892A>G XP_011531331.1:p.Asp631Gly
XM_011533030.2:c.1889A>G XP_011531332.1:p.Asp630Gly
XR_001738891.1:n.2396A>G
XR_939707.2:n.2396A>G
NM_022437.3:c.1880A>G MANE Select NP_071882.1:p.Asp627Gly
NM_001357321.2:c.1877A>G NP_001344250.1:p.Asp626Gly