Canonical Allele Identifier: CA2493965093

Gene: ABCG8

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43877722G= , CM000664.2:g.43877722G=	GRCh38
NC_000002.11:g.44104861G= , CM000664.1:g.44104861G=	GRCh37
NC_000002.10:g.43958365G=	NCBI36
NG_008884.1:g.43759G=
NG_008884.2:g.50781G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000272286.4:c.1884+34G= MANE Select	ENSP00000272286.2:n.1884+34G=
ENST00000272286.2:c.1884+34G=	ENSP00000272286.2:n.1884+34G=
NM_022437.2:c.1884+34G=	NP_071882.1:n.1884+34G=
XM_005264483.2:c.1881+34G=	XP_005264540.1:n.1881+34G=
XM_011533029.1:c.1896+34G=	XP_011531331.1:n.1896+34G=
XM_011533030.1:c.1893+34G=	XP_011531332.1:n.1893+34G=
XM_011533031.1:c.1668+34G=	XP_011531333.1:n.1668+34G=
XR_939707.1:n.2386+34G=
NM_001357321.1:c.1881+34G=	NP_001344250.1:n.1881+34G=
XM_011533029.2:c.1896+34G=	XP_011531331.1:n.1896+34G=
XM_011533030.2:c.1893+34G=	XP_011531332.1:n.1893+34G=
XR_001738891.1:n.2400+34G=
XR_939707.2:n.2400+34G=
NM_022437.3:c.1884+34G= MANE Select	NP_071882.1:n.1884+34G=
NM_001357321.2:c.1881+34G=	NP_001344250.1:n.1881+34G=