Canonical Allele Identifier: CA1637118

Gene: ABCG8

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43852491G>C , CM000664.2:g.43852491G>C	GRCh38
NC_000002.11:g.44079630G>C , CM000664.1:g.44079630G>C	GRCh37
NC_000002.10:g.43933134G>C	NCBI36
NG_008884.1:g.18528G>C
NG_008884.2:g.25550G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_022437.3:c.694+5G>C MANE Select	NP_071882.1:n.694+5G>C
ENST00000272286.4:c.694+5G>C MANE Select	ENSP00000272286.2:n.694+5G>C
NM_001357321.1:c.694+5G>C	NP_001344250.1:n.694+5G>C
NM_001357321.2:c.694+5G>C	NP_001344250.1:n.694+5G>C
NM_022437.2:c.694+5G>C	NP_071882.1:n.694+5G>C
ENST00000272286.2:c.694+5G>C	ENSP00000272286.2:n.694+5G>C
ENST00000644611.1:c.706+5G>C	ENSP00000495423.1:n.706+5G>C
XM_005264483.2:c.694+5G>C	XP_005264540.1:n.694+5G>C
XM_011533029.1:c.706+5G>C	XP_011531331.1:n.706+5G>C
XM_011533029.2:c.706+5G>C	XP_011531331.1:n.706+5G>C
XM_011533030.1:c.706+5G>C	XP_011531332.1:n.706+5G>C
XM_011533030.2:c.706+5G>C	XP_011531332.1:n.706+5G>C
XM_011533031.1:c.478+5G>C	XP_011531333.1:n.478+5G>C
XR_001738891.1:n.1210+5G>C
XR_939707.1:n.1196+5G>C
XR_939707.2:n.1210+5G>C