Canonical Allele Identifier: CA425752523

Gene: ABCG8

Linked Data

• MyVariant Identifiers: chr2:g.44073410A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43846271A>G , CM000664.2:g.43846271A>G	GRCh38
NC_000002.11:g.44073410A>G , CM000664.1:g.44073410A>G	GRCh37
NC_000002.10:g.43926914A>G	NCBI36
NG_008884.1:g.12308A>G
NG_008884.2:g.19330A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272286.4:c.282A>G MANE Select	ENSP00000272286.2:p.Lys94=
ENST00000643284.1:n.739A>G
ENST00000644611.1:c.294A>G	ENSP00000495423.1:p.Lys98=
ENST00000272286.2:c.282A>G	ENSP00000272286.2:p.Lys94=
NM_022437.2:c.282A>G	NP_071882.1:p.Lys94=
XM_005264483.2:c.282A>G	XP_005264540.1:p.Lys94=
XM_011533029.1:c.294A>G	XP_011531331.1:p.Lys98=
XM_011533030.1:c.294A>G	XP_011531332.1:p.Lys98=
XM_011533031.1:c.66A>G	XP_011531333.1:p.Lys22=
XR_939707.1:n.784A>G
NM_001357321.1:c.282A>G	NP_001344250.1:p.Lys94=
XM_011533029.2:c.294A>G	XP_011531331.1:p.Lys98=
XM_011533030.2:c.294A>G	XP_011531332.1:p.Lys98=
XR_001738891.1:n.798A>G
XR_939707.2:n.798A>G
NM_022437.3:c.282A>G MANE Select	NP_071882.1:p.Lys94=
NM_001357321.2:c.282A>G	NP_001344250.1:p.Lys94=