Canonical Allele Identifier: CA1789667997
Gene: CYP7B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.64624414A= , CM000670.2:g.64624414A= GRCh38
NC_000008.10:g.65536971A= , CM000670.1:g.65536971A= GRCh37
NC_000008.9:g.65699525A= NCBI36
NG_008338.1:g.179378T=
NG_008338.2:g.179378T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000310193.4:c.248T= MANE Select ENSP00000310721.3:p.Val83=
ENST00000310193.3:c.248T= ENSP00000310721.3:p.Val83=
NM_004820.3:c.248T= NP_004811.1:p.Val83=
NM_001324112.1:c.248T= NP_001311041.1:p.Val83=
NM_004820.4:c.248T= NP_004811.1:p.Val83=
XM_017014002.1:c.314T= XP_016869491.1:p.Val105=
NM_004820.5:c.248T= MANE Select NP_004811.1:p.Val83=
NM_001324112.2:c.248T= NP_001311041.1:p.Val83=