Canonical Allele Identifier: CA1637535

Gene: ABCG8

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43875190C>T , CM000664.2:g.43875190C>T	GRCh38
NC_000002.11:g.44102329C>T , CM000664.1:g.44102329C>T	GRCh37
NC_000002.10:g.43955833C>T	NCBI36
NG_008884.1:g.41227C>T
NG_008884.2:g.48249C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_022437.3:c.1533C>T MANE Select	NP_071882.1:p.Tyr511=
ENST00000272286.4:c.1533C>T MANE Select	ENSP00000272286.2:p.Tyr511=
NM_001357321.1:c.1530C>T	NP_001344250.1:p.Tyr510=
NM_001357321.2:c.1530C>T	NP_001344250.1:p.Tyr510=
NM_022437.2:c.1533C>T	NP_071882.1:p.Tyr511=
ENST00000272286.2:c.1533C>T	ENSP00000272286.2:p.Tyr511=
XM_005264483.2:c.1530C>T	XP_005264540.1:p.Tyr510=
XM_011533029.1:c.1545C>T	XP_011531331.1:p.Tyr515=
XM_011533029.2:c.1545C>T	XP_011531331.1:p.Tyr515=
XM_011533030.1:c.1542C>T	XP_011531332.1:p.Tyr514=
XM_011533030.2:c.1542C>T	XP_011531332.1:p.Tyr514=
XM_011533031.1:c.1317C>T	XP_011531333.1:p.Tyr439=
XR_001738891.1:n.2049C>T
XR_939707.1:n.2035C>T
XR_939707.2:n.2049C>T