Canonical Allele Identifier: CA1789664460
Gene: CYP7B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.64616106C= , CM000670.2:g.64616106C= GRCh38
NC_000008.10:g.65528663C= , CM000670.1:g.65528663C= GRCh37
NC_000008.9:g.65691217C= NCBI36
NG_008338.1:g.187686G=
NG_008338.2:g.187686G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000310193.4:c.435G= MANE Select ENSP00000310721.3:p.Leu145=
ENST00000310193.3:c.435G= ENSP00000310721.3:p.Leu145=
NM_004820.3:c.435G= NP_004811.1:p.Leu145=
NM_001324112.1:c.435G= NP_001311041.1:p.Leu145=
NM_004820.4:c.435G= NP_004811.1:p.Leu145=
XM_017014002.1:c.501G= XP_016869491.1:p.Leu167=
NM_004820.5:c.435G= MANE Select NP_004811.1:p.Leu145=
NM_001324112.2:c.435G= NP_001311041.1:p.Leu145=