Canonical Allele Identifier: CA1789711737
Gene: CYP7B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.64727531A= , CM000670.2:g.64727531A= GRCh38
NC_000008.10:g.65640088A= , CM000670.1:g.65640088A= GRCh37
NC_000008.9:g.65802642A= NCBI36
NG_008338.1:g.76261T=
NG_008338.2:g.76261T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000310193.4:c.122+70935T= MANE Select ENSP00000310721.3:n.122+70935T=
ENST00000310193.3:c.122+70935T= ENSP00000310721.3:n.122+70935T=
NM_004820.3:c.122+70935T= NP_004811.1:n.122+70935T=
NM_001324112.1:c.122+70935T= NP_001311041.1:n.122+70935T=
NM_004820.4:c.122+70935T= NP_004811.1:n.122+70935T=
NM_004820.5:c.122+70935T= MANE Select NP_004811.1:n.122+70935T=
NM_001324112.2:c.122+70935T= NP_001311041.1:n.122+70935T=