Canonical Allele Identifier: CA1789659742
Gene: CYP7B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.64604838A= , CM000670.2:g.64604838A= GRCh38
NC_000008.10:g.65517395A= , CM000670.1:g.65517395A= GRCh37
NC_000008.9:g.65679949A= NCBI36
NG_008338.1:g.198954T=
NG_008338.2:g.198954T=

Transcript Alleles

HGVS Amino-acid change
ENST00000310193.4:c.1077T= MANE Select ENSP00000310721.3:p.Ala359=
ENST00000310193.3:c.1077T= ENSP00000310721.3:p.Ala359=
ENST00000523954.1:n.351T=
NM_004820.3:c.1077T= NP_004811.1:p.Ala359=
NM_001324112.1:c.1077T= NP_001311041.1:p.Ala359=
NM_004820.4:c.1077T= NP_004811.1:p.Ala359=
XM_017014002.1:c.1143T= XP_016869491.1:p.Ala381=
NM_004820.5:c.1077T= MANE Select NP_004811.1:p.Ala359=
NM_001324112.2:c.1077T= NP_001311041.1:p.Ala359=