Canonical Allele Identifier: CA179054410
Gene: CYP7B1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10808739

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.64727703G>A , CM000670.2:g.64727703G>A GRCh38
NC_000008.10:g.65640260G>A , CM000670.1:g.65640260G>A GRCh37
NC_000008.9:g.65802814G>A NCBI36
NG_008338.1:g.76089C>T
NG_008338.2:g.76089C>T

Transcript Alleles

HGVS Amino-acid change
NM_004820.3:c.122+70763C>T VV NP_004811.1:p.=
NM_001324112.1:c.122+70763C>T VV NP_001311041.1:p.=
NM_004820.4:c.122+70763C>T VV
NM_004820.5:c.122+70763C>T VV MANE Preferred
ENST00000310193.3:c.122+70763C>T ENSP00000310721.3:p.=