Canonical Allele Identifier: CA651842110

Gene: CYP7B1

Linked Data

• COSMIC: COSN26619007

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.64624269T>A , CM000670.2:g.64624269T>A	GRCh38
NC_000008.10:g.65536826T>A , CM000670.1:g.65536826T>A	GRCh37
NC_000008.9:g.65699380T>A	NCBI36
NG_008338.1:g.179523A>T
NG_008338.2:g.179523A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310193.4:c.259+134A>T MANE Select	ENSP00000310721.3:n.259+134A>T
ENST00000310193.3:c.259+134A>T	ENSP00000310721.3:n.259+134A>T
NM_004820.3:c.259+134A>T	NP_004811.1:n.259+134A>T
NM_001324112.1:c.259+134A>T	NP_001311041.1:n.259+134A>T
NM_004820.4:c.259+134A>T	NP_004811.1:n.259+134A>T
XM_017014002.1:c.325+134A>T	XP_016869491.1:n.325+134A>T
NM_004820.5:c.259+134A>T MANE Select	NP_004811.1:n.259+134A>T
NM_001324112.2:c.259+134A>T	NP_001311041.1:n.259+134A>T