Canonical Allele Identifier: CA371334091

Gene: CYP7B1

Linked Data

• MyVariant Identifiers: chr8:g.65517288A>G (hg19) ; chr8:g.64604731A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.64604731A>G , CM000670.2:g.64604731A>G	GRCh38
NC_000008.10:g.65517288A>G , CM000670.1:g.65517288A>G	GRCh37
NC_000008.9:g.65679842A>G	NCBI36
NG_008338.1:g.199061T>C
NG_008338.2:g.199061T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000310193.4:c.1184T>C MANE Select	ENSP00000310721.3:p.Ile395Thr
ENST00000310193.3:c.1184T>C	ENSP00000310721.3:p.Ile395Thr
ENST00000523954.1:n.458T>C
NM_004820.3:c.1184T>C	NP_004811.1:p.Ile395Thr
NM_001324112.1:c.1184T>C	NP_001311041.1:p.Ile395Thr
NM_004820.4:c.1184T>C	NP_004811.1:p.Ile395Thr
XM_017014002.1:c.1250T>C	XP_016869491.1:p.Ile417Thr
NM_004820.5:c.1184T>C MANE Select	NP_004811.1:p.Ile395Thr
NM_001324112.2:c.1184T>C	NP_001311041.1:p.Ile395Thr