Canonical Allele Identifier: CA4764209
Gene: CYP7B1 HGNC NCBI

Linked Data

dbSNP Id: rs751354767
gnomAD v2: 8-65528657-G-A
gnomAD v4: 8-64616100-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.64616100G>A , CM000670.2:g.64616100G>A GRCh38
NC_000008.10:g.65528657G>A , CM000670.1:g.65528657G>A GRCh37
NC_000008.9:g.65691211G>A NCBI36
NG_008338.1:g.187692C>T
NG_008338.2:g.187692C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000310193.4:c.441C>T MANE Select ENSP00000310721.3:p.Gly147=
ENST00000310193.3:c.441C>T ENSP00000310721.3:p.Gly147=
NM_004820.3:c.441C>T NP_004811.1:p.Gly147=
NM_001324112.1:c.441C>T NP_001311041.1:p.Gly147=
NM_004820.4:c.441C>T NP_004811.1:p.Gly147=
XM_017014002.1:c.507C>T XP_016869491.1:p.Gly169=
NM_004820.5:c.441C>T MANE Select NP_004811.1:p.Gly147=
NM_001324112.2:c.441C>T NP_001311041.1:p.Gly147=