Canonical Allele Identifier: CA1789668023
Gene: CYP7B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.64624475G= , CM000670.2:g.64624475G= GRCh38
NC_000008.10:g.65537032G= , CM000670.1:g.65537032G= GRCh37
NC_000008.9:g.65699586G= NCBI36
NG_008338.1:g.179317C=
NG_008338.2:g.179317C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000310193.4:c.187C= MANE Select ENSP00000310721.3:p.Arg63=
ENST00000310193.3:c.187C= ENSP00000310721.3:p.Arg63=
NM_004820.3:c.187C= NP_004811.1:p.Arg63=
NM_001324112.1:c.187C= NP_001311041.1:p.Arg63=
NM_004820.4:c.187C= NP_004811.1:p.Arg63=
XM_017014002.1:c.253C= XP_016869491.1:p.Arg85=
NM_004820.5:c.187C= MANE Select NP_004811.1:p.Arg63=
NM_001324112.2:c.187C= NP_001311041.1:p.Arg63=