Canonical Allele Identifier: CA346670473

Gene: ABCG8

Linked Data

• MyVariant Identifiers: chr2:g.44102422C>G (hg19) ; chr2:g.43875283C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43875283C>G , CM000664.2:g.43875283C>G	GRCh38
NC_000002.11:g.44102422C>G , CM000664.1:g.44102422C>G	GRCh37
NC_000002.10:g.43955926C>G	NCBI36
NG_008884.1:g.41320C>G
NG_008884.2:g.48342C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000272286.4:c.1626C>G MANE Select	ENSP00000272286.2:p.Cys542Trp
ENST00000272286.2:c.1626C>G	ENSP00000272286.2:p.Cys542Trp
NM_022437.2:c.1626C>G	NP_071882.1:p.Cys542Trp
XM_005264483.2:c.1623C>G	XP_005264540.1:p.Cys541Trp
XM_011533029.1:c.1638C>G	XP_011531331.1:p.Cys546Trp
XM_011533030.1:c.1635C>G	XP_011531332.1:p.Cys545Trp
XM_011533031.1:c.1410C>G	XP_011531333.1:p.Cys470Trp
XR_939707.1:n.2128C>G
NM_001357321.1:c.1623C>G	NP_001344250.1:p.Cys541Trp
XM_011533029.2:c.1638C>G	XP_011531331.1:p.Cys546Trp
XM_011533030.2:c.1635C>G	XP_011531332.1:p.Cys545Trp
XR_001738891.1:n.2142C>G
XR_939707.2:n.2142C>G
NM_022437.3:c.1626C>G MANE Select	NP_071882.1:p.Cys542Trp
NM_001357321.2:c.1623C>G	NP_001344250.1:p.Cys541Trp