Canonical Allele Identifier: CA1789668050
Gene: CYP7B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.64624543C= , CM000670.2:g.64624543C= GRCh38
NC_000008.10:g.65537100C= , CM000670.1:g.65537100C= GRCh37
NC_000008.9:g.65699654C= NCBI36
NG_008338.1:g.179249G=
NG_008338.2:g.179249G=

Transcript Alleles

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