Canonical Allele Identifier: CA346670548

Gene: ABCG8

Linked Data

• MyVariant Identifiers: chr2:g.44102465C>A (hg19) ; chr2:g.43875326C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43875326C>A , CM000664.2:g.43875326C>A	GRCh38
NC_000002.11:g.44102465C>A , CM000664.1:g.44102465C>A	GRCh37
NC_000002.10:g.43955969C>A	NCBI36
NG_008884.1:g.41363C>A
NG_008884.2:g.48385C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272286.4:c.1669C>A MANE Select	ENSP00000272286.2:p.His557Asn
ENST00000272286.2:c.1669C>A	ENSP00000272286.2:p.His557Asn
NM_022437.2:c.1669C>A	NP_071882.1:p.His557Asn
XM_005264483.2:c.1666C>A	XP_005264540.1:p.His556Asn
XM_011533029.1:c.1681C>A	XP_011531331.1:p.His561Asn
XM_011533030.1:c.1678C>A	XP_011531332.1:p.His560Asn
XM_011533031.1:c.1453C>A	XP_011531333.1:p.His485Asn
XR_939707.1:n.2171C>A
NM_001357321.1:c.1666C>A	NP_001344250.1:p.His556Asn
XM_011533029.2:c.1681C>A	XP_011531331.1:p.His561Asn
XM_011533030.2:c.1678C>A	XP_011531332.1:p.His560Asn
XR_001738891.1:n.2185C>A
XR_939707.2:n.2185C>A
NM_022437.3:c.1669C>A MANE Select	NP_071882.1:p.His557Asn
NM_001357321.2:c.1666C>A	NP_001344250.1:p.His556Asn