Canonical Allele Identifier: CA461420347

Gene: CYP7B1

Linked Data

• MyVariant Identifiers: chr8:g.65528579T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.64616022T>G , CM000670.2:g.64616022T>G	GRCh38
NC_000008.10:g.65528579T>G , CM000670.1:g.65528579T>G	GRCh37
NC_000008.9:g.65691133T>G	NCBI36
NG_008338.1:g.187770A>C
NG_008338.2:g.187770A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310193.4:c.519A>C MANE Select	ENSP00000310721.3:p.Thr173=
ENST00000310193.3:c.519A>C	ENSP00000310721.3:p.Thr173=
NM_004820.3:c.519A>C	NP_004811.1:p.Thr173=
NM_001324112.1:c.519A>C	NP_001311041.1:p.Thr173=
NM_004820.4:c.519A>C	NP_004811.1:p.Thr173=
XM_017014002.1:c.585A>C	XP_016869491.1:p.Thr195=
NM_004820.5:c.519A>C MANE Select	NP_004811.1:p.Thr173=
NM_001324112.2:c.519A>C	NP_001311041.1:p.Thr173=