Canonical Allele Identifier: CA2493965072
Gene: ABCG8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43877687A= , CM000664.2:g.43877687A= GRCh38
NC_000002.11:g.44104826A= , CM000664.1:g.44104826A= GRCh37
NC_000002.10:g.43958330A= NCBI36
NG_008884.1:g.43724A=
NG_008884.2:g.50746A=

Transcript Alleles

HGVS Amino-acid change
ENST00000272286.4:c.1883A= MANE Select ENSP00000272286.2:p.Lys628=
ENST00000272286.2:c.1883A= ENSP00000272286.2:p.Lys628=
NM_022437.2:c.1883A= NP_071882.1:p.Lys628=
XM_005264483.2:c.1880A= XP_005264540.1:p.Lys627=
XM_011533029.1:c.1895A= XP_011531331.1:p.Lys632=
XM_011533030.1:c.1892A= XP_011531332.1:p.Lys631=
XM_011533031.1:c.1667A= XP_011531333.1:p.Lys556=
XR_939707.1:n.2385A=
NM_001357321.1:c.1880A= NP_001344250.1:p.Lys627=
XM_011533029.2:c.1895A= XP_011531331.1:p.Lys632=
XM_011533030.2:c.1892A= XP_011531332.1:p.Lys631=
XR_001738891.1:n.2399A=
XR_939707.2:n.2399A=
NM_022437.3:c.1883A= MANE Select NP_071882.1:p.Lys628=
NM_001357321.2:c.1880A= NP_001344250.1:p.Lys627=