Canonical Allele Identifier: CA1789659693
Gene: CYP7B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.64604732T= , CM000670.2:g.64604732T= GRCh38
NC_000008.10:g.65517289T= , CM000670.1:g.65517289T= GRCh37
NC_000008.9:g.65679843T= NCBI36
NG_008338.1:g.199060A=
NG_008338.2:g.199060A=

Transcript Alleles

HGVS Amino-acid change
ENST00000310193.4:c.1183A= MANE Select ENSP00000310721.3:p.Ile395=
ENST00000310193.3:c.1183A= ENSP00000310721.3:p.Ile395=
ENST00000523954.1:n.457A=
NM_004820.3:c.1183A= NP_004811.1:p.Ile395=
NM_001324112.1:c.1183A= NP_001311041.1:p.Ile395=
NM_004820.4:c.1183A= NP_004811.1:p.Ile395=
XM_017014002.1:c.1249A= XP_016869491.1:p.Ile417=
NM_004820.5:c.1183A= MANE Select NP_004811.1:p.Ile395=
NM_001324112.2:c.1183A= NP_001311041.1:p.Ile395=