Canonical Allele Identifier: CA346670553

Gene: ABCG8

Linked Data

• MyVariant Identifiers: chr2:g.44102466A>C (hg19) ; chr2:g.43875327A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43875327A>C , CM000664.2:g.43875327A>C	GRCh38
NC_000002.11:g.44102466A>C , CM000664.1:g.44102466A>C	GRCh37
NC_000002.10:g.43955970A>C	NCBI36
NG_008884.1:g.41364A>C
NG_008884.2:g.48386A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272286.4:c.1670A>C MANE Select	ENSP00000272286.2:p.His557Pro
ENST00000272286.2:c.1670A>C	ENSP00000272286.2:p.His557Pro
NM_022437.2:c.1670A>C	NP_071882.1:p.His557Pro
XM_005264483.2:c.1667A>C	XP_005264540.1:p.His556Pro
XM_011533029.1:c.1682A>C	XP_011531331.1:p.His561Pro
XM_011533030.1:c.1679A>C	XP_011531332.1:p.His560Pro
XM_011533031.1:c.1454A>C	XP_011531333.1:p.His485Pro
XR_939707.1:n.2172A>C
NM_001357321.1:c.1667A>C	NP_001344250.1:p.His556Pro
XM_011533029.2:c.1682A>C	XP_011531331.1:p.His561Pro
XM_011533030.2:c.1679A>C	XP_011531332.1:p.His560Pro
XR_001738891.1:n.2186A>C
XR_939707.2:n.2186A>C
NM_022437.3:c.1670A>C MANE Select	NP_071882.1:p.His557Pro
NM_001357321.2:c.1667A>C	NP_001344250.1:p.His556Pro