Canonical Allele Identifier: CA1637371

Gene: ABCG8

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43873801A>G , CM000664.2:g.43873801A>G	GRCh38
NC_000002.11:g.44100940A>G , CM000664.1:g.44100940A>G	GRCh37
NC_000002.10:g.43954444A>G	NCBI36
NG_008884.1:g.39838A>G
NG_008884.2:g.46860A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_022437.3:c.1226A>G MANE Select	NP_071882.1:p.Asn409Ser
ENST00000272286.4:c.1226A>G MANE Select	ENSP00000272286.2:p.Asn409Ser
NM_001357321.1:c.1223A>G	NP_001344250.1:p.Asn408Ser
NM_001357321.2:c.1223A>G	NP_001344250.1:p.Asn408Ser
NM_022437.2:c.1226A>G	NP_071882.1:p.Asn409Ser
ENST00000272286.2:c.1226A>G	ENSP00000272286.2:p.Asn409Ser
ENST00000644611.1:c.1238A>G	ENSP00000495423.1:p.Asn413Ser
XM_005264483.2:c.1223A>G	XP_005264540.1:p.Asn408Ser
XM_011533029.1:c.1238A>G	XP_011531331.1:p.Asn413Ser
XM_011533029.2:c.1238A>G	XP_011531331.1:p.Asn413Ser
XM_011533030.1:c.1235A>G	XP_011531332.1:p.Asn412Ser
XM_011533030.2:c.1235A>G	XP_011531332.1:p.Asn412Ser
XM_011533031.1:c.1010A>G	XP_011531333.1:p.Asn337Ser
XR_001738891.1:n.1742A>G
XR_939707.1:n.1728A>G
XR_939707.2:n.1742A>G