Canonical Allele Identifier: CA425908339

Gene: ABCG8

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43877865C>T , CM000664.2:g.43877865C>T	GRCh38
NC_000002.11:g.44105004C>T , CM000664.1:g.44105004C>T	GRCh37
NC_000002.10:g.43958508C>T	NCBI36
NG_008884.1:g.43902C>T
NG_008884.2:g.50924C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272286.4:c.1974C>T MANE Select	ENSP00000272286.2:p.Tyr658=
ENST00000272286.2:c.1974C>T	ENSP00000272286.2:p.Tyr658=
NM_022437.2:c.1974C>T	NP_071882.1:p.Tyr658=
XM_005264483.2:c.1971C>T	XP_005264540.1:p.Tyr657=
XM_011533029.1:c.1986C>T	XP_011531331.1:p.Tyr662=
XM_011533030.1:c.1983C>T	XP_011531332.1:p.Tyr661=
XM_011533031.1:c.1758C>T	XP_011531333.1:p.Tyr586=
XR_939707.1:n.2476C>T
NM_001357321.1:c.1971C>T	NP_001344250.1:p.Tyr657=
XM_011533029.2:c.1986C>T	XP_011531331.1:p.Tyr662=
XM_011533030.2:c.1983C>T	XP_011531332.1:p.Tyr661=
XR_001738891.1:n.2490C>T
XR_939707.2:n.2490C>T
NM_022437.3:c.1974C>T MANE Select	NP_071882.1:p.Tyr658=
NM_001357321.2:c.1971C>T	NP_001344250.1:p.Tyr657=