Canonical Allele Identifier: CA346666578

Gene: ABCG8

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43852690C>G , CM000664.2:g.43852690C>G	GRCh38
NC_000002.11:g.44079829C>G , CM000664.1:g.44079829C>G	GRCh37
NC_000002.10:g.43933333C>G	NCBI36
NG_008884.1:g.18727C>G
NG_008884.2:g.25749C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_022437.3:c.786C>G MANE Select	NP_071882.1:p.Asn262Lys
ENST00000272286.4:c.786C>G MANE Select	ENSP00000272286.2:p.Asn262Lys
NM_001357321.1:c.786C>G	NP_001344250.1:p.Asn262Lys
NM_001357321.2:c.786C>G	NP_001344250.1:p.Asn262Lys
NM_022437.2:c.786C>G	NP_071882.1:p.Asn262Lys
ENST00000272286.2:c.786C>G	ENSP00000272286.2:p.Asn262Lys
ENST00000644611.1:c.798C>G	ENSP00000495423.1:p.Asn266Lys
XM_005264483.2:c.786C>G	XP_005264540.1:p.Asn262Lys
XM_011533029.1:c.798C>G	XP_011531331.1:p.Asn266Lys
XM_011533029.2:c.798C>G	XP_011531331.1:p.Asn266Lys
XM_011533030.1:c.798C>G	XP_011531332.1:p.Asn266Lys
XM_011533030.2:c.798C>G	XP_011531332.1:p.Asn266Lys
XM_011533031.1:c.570C>G	XP_011531333.1:p.Asn190Lys
XR_001738891.1:n.1302C>G
XR_939707.1:n.1288C>G
XR_939707.2:n.1302C>G