Canonical Allele Identifier: CA371335696

Gene: CYP7B1

Linked Data

• COSMIC: COSM3663832
• MyVariant Identifiers: chr8:g.65528635C>A (hg19) ; chr8:g.64616078C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.64616078C>A , CM000670.2:g.64616078C>A	GRCh38
NC_000008.10:g.65528635C>A , CM000670.1:g.65528635C>A	GRCh37
NC_000008.9:g.65691189C>A	NCBI36
NG_008338.1:g.187714G>T
NG_008338.2:g.187714G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310193.4:c.463G>T MANE Select	ENSP00000310721.3:p.Glu155Ter
ENST00000310193.3:c.463G>T	ENSP00000310721.3:p.Glu155Ter
NM_004820.3:c.463G>T	NP_004811.1:p.Glu155Ter
NM_001324112.1:c.463G>T	NP_001311041.1:p.Glu155Ter
NM_004820.4:c.463G>T	NP_004811.1:p.Glu155Ter
XM_017014002.1:c.529G>T	XP_016869491.1:p.Glu177Ter
NM_004820.5:c.463G>T MANE Select	NP_004811.1:p.Glu155Ter
NM_001324112.2:c.463G>T	NP_001311041.1:p.Glu155Ter