Canonical Allele Identifier: CA2493941103
Gene: ABCG8 HGNC NCBI

Linked Data

dbSNP Id: rs1572812616

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43838956T>G , CM000664.2:g.43838956T>G GRCh38
NC_000002.11:g.44066095T>G , CM000664.1:g.44066095T>G GRCh37
NC_000002.10:g.43919599T>G NCBI36
NG_008883.1:g.4864A>C
NG_008884.1:g.4993T>G
NG_008884.2:g.12015T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000643284.1:n.521-5551T>G
ENST00000644611.1:c.76-5551T>G ENSP00000495423.1:n.76-5551T>G
XM_011533029.1:c.76-5551T>G XP_011531331.1:n.76-5551T>G
XM_011533030.1:c.76-5551T>G XP_011531332.1:n.76-5551T>G
XM_011533031.1:c.-153-5551T>G XP_011531333.1:n.-153-5551T>G
XR_939707.1:n.566-5551T>G
XM_011533029.2:c.76-5551T>G XP_011531331.1:n.76-5551T>G
XM_011533030.2:c.76-5551T>G XP_011531332.1:n.76-5551T>G
XR_001738891.1:n.580-5551T>G
XR_939707.2:n.580-5551T>G