Canonical Allele Identifier: CA371334102
Gene: CYP7B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.64604737A>T , CM000670.2:g.64604737A>T GRCh38
NC_000008.10:g.65517294A>T , CM000670.1:g.65517294A>T GRCh37
NC_000008.9:g.65679848A>T NCBI36
NG_008338.1:g.199055T>A
NG_008338.2:g.199055T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000310193.4:c.1178T>A MANE Select ENSP00000310721.3:p.Val393Glu
ENST00000310193.3:c.1178T>A ENSP00000310721.3:p.Val393Glu
ENST00000523954.1:n.452T>A
NM_004820.3:c.1178T>A NP_004811.1:p.Val393Glu
NM_001324112.1:c.1178T>A NP_001311041.1:p.Val393Glu
NM_004820.4:c.1178T>A NP_004811.1:p.Val393Glu
XM_017014002.1:c.1244T>A XP_016869491.1:p.Val415Glu
NM_004820.5:c.1178T>A MANE Select NP_004811.1:p.Val393Glu
NM_001324112.2:c.1178T>A NP_001311041.1:p.Val393Glu