Canonical Allele Identifier: CA178391955
Gene: CYP7B1 HGNC NCBI

Linked Data

dbSNP Id: rs867209693
gnomAD v2: 8-65537059-G-A
gnomAD v4: 8-64624502-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.64624502G>A , CM000670.2:g.64624502G>A GRCh38
NC_000008.10:g.65537059G>A , CM000670.1:g.65537059G>A GRCh37
NC_000008.9:g.65699613G>A NCBI36
NG_008338.1:g.179290C>T
NG_008338.2:g.179290C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000310193.4:c.160C>T MANE Select ENSP00000310721.3:p.Pro54Ser
ENST00000310193.3:c.160C>T ENSP00000310721.3:p.Pro54Ser
NM_004820.3:c.160C>T NP_004811.1:p.Pro54Ser
NM_001324112.1:c.160C>T NP_001311041.1:p.Pro54Ser
NM_004820.4:c.160C>T NP_004811.1:p.Pro54Ser
XM_017014002.1:c.226C>T XP_016869491.1:p.Pro76Ser
NM_004820.5:c.160C>T MANE Select NP_004811.1:p.Pro54Ser
NM_001324112.2:c.160C>T NP_001311041.1:p.Pro54Ser