Canonical Allele Identifier: CA461121038

Gene: CYP7B1

Linked Data

• MyVariant Identifiers: chr8:g.65537045C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.64624488C>G , CM000670.2:g.64624488C>G	GRCh38
NC_000008.10:g.65537045C>G , CM000670.1:g.65537045C>G	GRCh37
NC_000008.9:g.65699599C>G	NCBI36
NG_008338.1:g.179304G>C
NG_008338.2:g.179304G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310193.4:c.174G>C MANE Select	ENSP00000310721.3:p.Val58=
ENST00000310193.3:c.174G>C	ENSP00000310721.3:p.Val58=
NM_004820.3:c.174G>C	NP_004811.1:p.Val58=
NM_001324112.1:c.174G>C	NP_001311041.1:p.Val58=
NM_004820.4:c.174G>C	NP_004811.1:p.Val58=
XM_017014002.1:c.240G>C	XP_016869491.1:p.Val80=
NM_004820.5:c.174G>C MANE Select	NP_004811.1:p.Val58=
NM_001324112.2:c.174G>C	NP_001311041.1:p.Val58=