Canonical Allele Identifier: CA2493965086
Gene: ABCG8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43877709G= , CM000664.2:g.43877709G= GRCh38
NC_000002.11:g.44104848G= , CM000664.1:g.44104848G= GRCh37
NC_000002.10:g.43958352G= NCBI36
NG_008884.1:g.43746G=
NG_008884.2:g.50768G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000272286.4:c.1884+21G= MANE Select ENSP00000272286.2:n.1884+21G=
ENST00000272286.2:c.1884+21G= ENSP00000272286.2:n.1884+21G=
NM_022437.2:c.1884+21G= NP_071882.1:n.1884+21G=
XM_005264483.2:c.1881+21G= XP_005264540.1:n.1881+21G=
XM_011533029.1:c.1896+21G= XP_011531331.1:n.1896+21G=
XM_011533030.1:c.1893+21G= XP_011531332.1:n.1893+21G=
XM_011533031.1:c.1668+21G= XP_011531333.1:n.1668+21G=
XR_939707.1:n.2386+21G=
NM_001357321.1:c.1881+21G= NP_001344250.1:n.1881+21G=
XM_011533029.2:c.1896+21G= XP_011531331.1:n.1896+21G=
XM_011533030.2:c.1893+21G= XP_011531332.1:n.1893+21G=
XR_001738891.1:n.2400+21G=
XR_939707.2:n.2400+21G=
NM_022437.3:c.1884+21G= MANE Select NP_071882.1:n.1884+21G=
NM_001357321.2:c.1881+21G= NP_001344250.1:n.1881+21G=