Canonical Allele Identifier: CA1789659739
Gene: CYP7B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.64604834G= , CM000670.2:g.64604834G= GRCh38
NC_000008.10:g.65517391G= , CM000670.1:g.65517391G= GRCh37
NC_000008.9:g.65679945G= NCBI36
NG_008338.1:g.198958C=
NG_008338.2:g.198958C=

Transcript Alleles

HGVS Amino-acid change
ENST00000310193.4:c.1081C= MANE Select ENSP00000310721.3:p.Arg361=
ENST00000310193.3:c.1081C= ENSP00000310721.3:p.Arg361=
ENST00000523954.1:n.355C=
NM_004820.3:c.1081C= NP_004811.1:p.Arg361=
NM_001324112.1:c.1081C= NP_001311041.1:p.Arg361=
NM_004820.4:c.1081C= NP_004811.1:p.Arg361=
XM_017014002.1:c.1147C= XP_016869491.1:p.Arg383=
NM_004820.5:c.1081C= MANE Select NP_004811.1:p.Arg361=
NM_001324112.2:c.1081C= NP_001311041.1:p.Arg361=