Canonical Allele Identifier: CA346663358

Gene: ABCG8

Linked Data

• MyVariant Identifiers: chr2:g.44071745C>A (hg19) ; chr2:g.43844606C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43844606C>A , CM000664.2:g.43844606C>A	GRCh38
NC_000002.11:g.44071745C>A , CM000664.1:g.44071745C>A	GRCh37
NC_000002.10:g.43925249C>A	NCBI36
NG_008884.1:g.10643C>A
NG_008884.2:g.17665C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000272286.4:c.163C>A MANE Select	ENSP00000272286.2:p.Gln55Lys
ENST00000643284.1:n.620C>A
ENST00000644611.1:c.175C>A	ENSP00000495423.1:p.Gln59Lys
ENST00000272286.2:c.163C>A	ENSP00000272286.2:p.Gln55Lys
NM_022437.2:c.163C>A	NP_071882.1:p.Gln55Lys
XM_005264483.2:c.163C>A	XP_005264540.1:p.Gln55Lys
XM_011533029.1:c.175C>A	XP_011531331.1:p.Gln59Lys
XM_011533030.1:c.175C>A	XP_011531332.1:p.Gln59Lys
XM_011533031.1:c.-54C>A	XP_011531333.1:n.-54C>A
XR_939707.1:n.665C>A
NM_001357321.1:c.163C>A	NP_001344250.1:p.Gln55Lys
XM_011533029.2:c.175C>A	XP_011531331.1:p.Gln59Lys
XM_011533030.2:c.175C>A	XP_011531332.1:p.Gln59Lys
XR_001738891.1:n.679C>A
XR_939707.2:n.679C>A
NM_022437.3:c.163C>A MANE Select	NP_071882.1:p.Gln55Lys
NM_001357321.2:c.163C>A	NP_001344250.1:p.Gln55Lys