Canonical Allele Identifier: CA1789659737
Gene: CYP7B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.64604830A= , CM000670.2:g.64604830A= GRCh38
NC_000008.10:g.65517387A= , CM000670.1:g.65517387A= GRCh37
NC_000008.9:g.65679941A= NCBI36
NG_008338.1:g.198962T=
NG_008338.2:g.198962T=

Transcript Alleles

HGVS Amino-acid change
ENST00000310193.4:c.1085T= MANE Select ENSP00000310721.3:p.Leu362=
ENST00000310193.3:c.1085T= ENSP00000310721.3:p.Leu362=
ENST00000523954.1:n.359T=
NM_004820.3:c.1085T= NP_004811.1:p.Leu362=
NM_001324112.1:c.1085T= NP_001311041.1:p.Leu362=
NM_004820.4:c.1085T= NP_004811.1:p.Leu362=
XM_017014002.1:c.1151T= XP_016869491.1:p.Leu384=
NM_004820.5:c.1085T= MANE Select NP_004811.1:p.Leu362=
NM_001324112.2:c.1085T= NP_001311041.1:p.Leu362=