Canonical Allele Identifier: CA1789659695
Gene: CYP7B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.64604735C= , CM000670.2:g.64604735C= GRCh38
NC_000008.10:g.65517292C= , CM000670.1:g.65517292C= GRCh37
NC_000008.9:g.65679846C= NCBI36
NG_008338.1:g.199057G=
NG_008338.2:g.199057G=

Transcript Alleles

HGVS Amino-acid change
ENST00000310193.4:c.1180G= MANE Select ENSP00000310721.3:p.Ala394=
ENST00000310193.3:c.1180G= ENSP00000310721.3:p.Ala394=
ENST00000523954.1:n.454G=
NM_004820.3:c.1180G= NP_004811.1:p.Ala394=
NM_001324112.1:c.1180G= NP_001311041.1:p.Ala394=
NM_004820.4:c.1180G= NP_004811.1:p.Ala394=
XM_017014002.1:c.1246G= XP_016869491.1:p.Ala416=
NM_004820.5:c.1180G= MANE Select NP_004811.1:p.Ala394=
NM_001324112.2:c.1180G= NP_001311041.1:p.Ala394=