Canonical Allele Identifier: CA346670617
Gene: ABCG8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43875356T>G , CM000664.2:g.43875356T>G GRCh38
NC_000002.11:g.44102495T>G , CM000664.1:g.44102495T>G GRCh37
NC_000002.10:g.43955999T>G NCBI36
NG_008884.1:g.41393T>G
NG_008884.2:g.48415T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000272286.4:c.1699T>G MANE Select ENSP00000272286.2:p.Tyr567Asp
ENST00000272286.2:c.1699T>G ENSP00000272286.2:p.Tyr567Asp
NM_022437.2:c.1699T>G NP_071882.1:p.Tyr567Asp
XM_005264483.2:c.1696T>G XP_005264540.1:p.Tyr566Asp
XM_011533029.1:c.1711T>G XP_011531331.1:p.Tyr571Asp
XM_011533030.1:c.1708T>G XP_011531332.1:p.Tyr570Asp
XM_011533031.1:c.1483T>G XP_011531333.1:p.Tyr495Asp
XR_939707.1:n.2201T>G
NM_001357321.1:c.1696T>G NP_001344250.1:p.Tyr566Asp
XM_011533029.2:c.1711T>G XP_011531331.1:p.Tyr571Asp
XM_011533030.2:c.1708T>G XP_011531332.1:p.Tyr570Asp
XR_001738891.1:n.2215T>G
XR_939707.2:n.2215T>G
NM_022437.3:c.1699T>G MANE Select NP_071882.1:p.Tyr567Asp
NM_001357321.2:c.1696T>G NP_001344250.1:p.Tyr566Asp