Canonical Allele Identifier: CA346663637

Gene: ABCG8

Linked Data

• MyVariant Identifiers: chr2:g.44073415G>C (hg19) ; chr2:g.43846276G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43846276G>C , CM000664.2:g.43846276G>C	GRCh38
NC_000002.11:g.44073415G>C , CM000664.1:g.44073415G>C	GRCh37
NC_000002.10:g.43926919G>C	NCBI36
NG_008884.1:g.12313G>C
NG_008884.2:g.19335G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272286.4:c.287G>C MANE Select	ENSP00000272286.2:p.Arg96Thr
ENST00000643284.1:n.744G>C
ENST00000644611.1:c.299G>C	ENSP00000495423.1:p.Arg100Thr
ENST00000272286.2:c.287G>C	ENSP00000272286.2:p.Arg96Thr
NM_022437.2:c.287G>C	NP_071882.1:p.Arg96Thr
XM_005264483.2:c.287G>C	XP_005264540.1:p.Arg96Thr
XM_011533029.1:c.299G>C	XP_011531331.1:p.Arg100Thr
XM_011533030.1:c.299G>C	XP_011531332.1:p.Arg100Thr
XM_011533031.1:c.71G>C	XP_011531333.1:p.Arg24Thr
XR_939707.1:n.789G>C
NM_001357321.1:c.287G>C	NP_001344250.1:p.Arg96Thr
XM_011533029.2:c.299G>C	XP_011531331.1:p.Arg100Thr
XM_011533030.2:c.299G>C	XP_011531332.1:p.Arg100Thr
XR_001738891.1:n.803G>C
XR_939707.2:n.803G>C
NM_022437.3:c.287G>C MANE Select	NP_071882.1:p.Arg96Thr
NM_001357321.2:c.287G>C	NP_001344250.1:p.Arg96Thr