Canonical Allele Identifier: CA346670840

Gene: ABCG8

Linked Data

• MyVariant Identifiers: chr2:g.44104745A>T (hg19) ; chr2:g.43877606A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43877606A>T , CM000664.2:g.43877606A>T	GRCh38
NC_000002.11:g.44104745A>T , CM000664.1:g.44104745A>T	GRCh37
NC_000002.10:g.43958249A>T	NCBI36
NG_008884.1:g.43643A>T
NG_008884.2:g.50665A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272286.4:c.1802A>T MANE Select	ENSP00000272286.2:p.Glu601Val
ENST00000272286.2:c.1802A>T	ENSP00000272286.2:p.Glu601Val
NM_022437.2:c.1802A>T	NP_071882.1:p.Glu601Val
XM_005264483.2:c.1799A>T	XP_005264540.1:p.Glu600Val
XM_011533029.1:c.1814A>T	XP_011531331.1:p.Glu605Val
XM_011533030.1:c.1811A>T	XP_011531332.1:p.Glu604Val
XM_011533031.1:c.1586A>T	XP_011531333.1:p.Glu529Val
XR_939707.1:n.2304A>T
NM_001357321.1:c.1799A>T	NP_001344250.1:p.Glu600Val
XM_011533029.2:c.1814A>T	XP_011531331.1:p.Glu605Val
XM_011533030.2:c.1811A>T	XP_011531332.1:p.Glu604Val
XR_001738891.1:n.2318A>T
XR_939707.2:n.2318A>T
NM_022437.3:c.1802A>T MANE Select	NP_071882.1:p.Glu601Val
NM_001357321.2:c.1799A>T	NP_001344250.1:p.Glu600Val