Canonical Allele Identifier: CA425908190

Gene: ABCG8

Linked Data

• MyVariant Identifiers: chr2:g.44104749G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43877610G>C , CM000664.2:g.43877610G>C	GRCh38
NC_000002.11:g.44104749G>C , CM000664.1:g.44104749G>C	GRCh37
NC_000002.10:g.43958253G>C	NCBI36
NG_008884.1:g.43647G>C
NG_008884.2:g.50669G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272286.4:c.1806G>C MANE Select	ENSP00000272286.2:p.Gly602=
ENST00000272286.2:c.1806G>C	ENSP00000272286.2:p.Gly602=
NM_022437.2:c.1806G>C	NP_071882.1:p.Gly602=
XM_005264483.2:c.1803G>C	XP_005264540.1:p.Gly601=
XM_011533029.1:c.1818G>C	XP_011531331.1:p.Gly606=
XM_011533030.1:c.1815G>C	XP_011531332.1:p.Gly605=
XM_011533031.1:c.1590G>C	XP_011531333.1:p.Gly530=
XR_939707.1:n.2308G>C
NM_001357321.1:c.1803G>C	NP_001344250.1:p.Gly601=
XM_011533029.2:c.1818G>C	XP_011531331.1:p.Gly606=
XM_011533030.2:c.1815G>C	XP_011531332.1:p.Gly605=
XR_001738891.1:n.2322G>C
XR_939707.2:n.2322G>C
NM_022437.3:c.1806G>C MANE Select	NP_071882.1:p.Gly602=
NM_001357321.2:c.1803G>C	NP_001344250.1:p.Gly601=