Canonical Allele Identifier: CA1789667950
Gene: CYP7B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.64624286A= , CM000670.2:g.64624286A= GRCh38
NC_000008.10:g.65536843A= , CM000670.1:g.65536843A= GRCh37
NC_000008.9:g.65699397A= NCBI36
NG_008338.1:g.179506T=
NG_008338.2:g.179506T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000310193.4:c.259+117T= MANE Select ENSP00000310721.3:n.259+117T=
ENST00000310193.3:c.259+117T= ENSP00000310721.3:n.259+117T=
NM_004820.3:c.259+117T= NP_004811.1:n.259+117T=
NM_001324112.1:c.259+117T= NP_001311041.1:n.259+117T=
NM_004820.4:c.259+117T= NP_004811.1:n.259+117T=
XM_017014002.1:c.325+117T= XP_016869491.1:n.325+117T=
NM_004820.5:c.259+117T= MANE Select NP_004811.1:n.259+117T=
NM_001324112.2:c.259+117T= NP_001311041.1:n.259+117T=