Canonical Allele Identifier: CA426116428

Gene: ABCG8

Linked Data

• MyVariant Identifiers: chr2:g.44102464C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43875325C>T , CM000664.2:g.43875325C>T	GRCh38
NC_000002.11:g.44102464C>T , CM000664.1:g.44102464C>T	GRCh37
NC_000002.10:g.43955968C>T	NCBI36
NG_008884.1:g.41362C>T
NG_008884.2:g.48384C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272286.4:c.1668C>T MANE Select	ENSP00000272286.2:p.Phe556=
ENST00000272286.2:c.1668C>T	ENSP00000272286.2:p.Phe556=
NM_022437.2:c.1668C>T	NP_071882.1:p.Phe556=
XM_005264483.2:c.1665C>T	XP_005264540.1:p.Phe555=
XM_011533029.1:c.1680C>T	XP_011531331.1:p.Phe560=
XM_011533030.1:c.1677C>T	XP_011531332.1:p.Phe559=
XM_011533031.1:c.1452C>T	XP_011531333.1:p.Phe484=
XR_939707.1:n.2170C>T
NM_001357321.1:c.1665C>T	NP_001344250.1:p.Phe555=
XM_011533029.2:c.1680C>T	XP_011531331.1:p.Phe560=
XM_011533030.2:c.1677C>T	XP_011531332.1:p.Phe559=
XR_001738891.1:n.2184C>T
XR_939707.2:n.2184C>T
NM_022437.3:c.1668C>T MANE Select	NP_071882.1:p.Phe556=
NM_001357321.2:c.1665C>T	NP_001344250.1:p.Phe555=