Canonical Allele Identifier: CA371335826
Gene: CYP7B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.64616134T>G , CM000670.2:g.64616134T>G GRCh38
NC_000008.10:g.65528691T>G , CM000670.1:g.65528691T>G GRCh37
NC_000008.9:g.65691245T>G NCBI36
NG_008338.1:g.187658A>C
NG_008338.2:g.187658A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000310193.4:c.407A>C MANE Select ENSP00000310721.3:p.Asp136Ala
ENST00000310193.3:c.407A>C ENSP00000310721.3:p.Asp136Ala
NM_004820.3:c.407A>C NP_004811.1:p.Asp136Ala
NM_001324112.1:c.407A>C NP_001311041.1:p.Asp136Ala
NM_004820.4:c.407A>C NP_004811.1:p.Asp136Ala
XM_017014002.1:c.473A>C XP_016869491.1:p.Asp158Ala
NM_004820.5:c.407A>C MANE Select NP_004811.1:p.Asp136Ala
NM_001324112.2:c.407A>C NP_001311041.1:p.Asp136Ala