Canonical Allele Identifier: CA461118314

Gene: CYP7B1

Linked Data

• MyVariant Identifiers: chr8:g.65517389T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.64604832T>A , CM000670.2:g.64604832T>A	GRCh38
NC_000008.10:g.65517389T>A , CM000670.1:g.65517389T>A	GRCh37
NC_000008.9:g.65679943T>A	NCBI36
NG_008338.1:g.198960A>T
NG_008338.2:g.198960A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000310193.4:c.1083A>T MANE Select	ENSP00000310721.3:p.Arg361=
ENST00000310193.3:c.1083A>T	ENSP00000310721.3:p.Arg361=
ENST00000523954.1:n.357A>T
NM_004820.3:c.1083A>T	NP_004811.1:p.Arg361=
NM_001324112.1:c.1083A>T	NP_001311041.1:p.Arg361=
NM_004820.4:c.1083A>T	NP_004811.1:p.Arg361=
XM_017014002.1:c.1149A>T	XP_016869491.1:p.Arg383=
NM_004820.5:c.1083A>T MANE Select	NP_004811.1:p.Arg361=
NM_001324112.2:c.1083A>T	NP_001311041.1:p.Arg361=