Canonical Allele Identifier: CA371335644
Gene: CYP7B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.64616057T>A , CM000670.2:g.64616057T>A GRCh38
NC_000008.10:g.65528614T>A , CM000670.1:g.65528614T>A GRCh37
NC_000008.9:g.65691168T>A NCBI36
NG_008338.1:g.187735A>T
NG_008338.2:g.187735A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000310193.4:c.484A>T MANE Select ENSP00000310721.3:p.Lys162Ter
ENST00000310193.3:c.484A>T ENSP00000310721.3:p.Lys162Ter
NM_004820.3:c.484A>T NP_004811.1:p.Lys162Ter
NM_001324112.1:c.484A>T NP_001311041.1:p.Lys162Ter
NM_004820.4:c.484A>T NP_004811.1:p.Lys162Ter
XM_017014002.1:c.550A>T XP_016869491.1:p.Lys184Ter
NM_004820.5:c.484A>T MANE Select NP_004811.1:p.Lys162Ter
NM_001324112.2:c.484A>T NP_001311041.1:p.Lys162Ter