Canonical Allele Identifier: CA1789668074
Gene: CYP7B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.64624580T= , CM000670.2:g.64624580T= GRCh38
NC_000008.10:g.65537137T= , CM000670.1:g.65537137T= GRCh37
NC_000008.9:g.65699691T= NCBI36
NG_008338.1:g.179212A=
NG_008338.2:g.179212A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000310193.4:c.123-41A= MANE Select ENSP00000310721.3:n.123-41A=
ENST00000310193.3:c.123-41A= ENSP00000310721.3:n.123-41A=
NM_004820.3:c.123-41A= NP_004811.1:n.123-41A=
NM_001324112.1:c.123-41A= NP_001311041.1:n.123-41A=
NM_004820.4:c.123-41A= NP_004811.1:n.123-41A=
XM_017014002.1:c.189-41A= XP_016869491.1:n.189-41A=
NM_004820.5:c.123-41A= MANE Select NP_004811.1:n.123-41A=
NM_001324112.2:c.123-41A= NP_001311041.1:n.123-41A=