Canonical Allele Identifier: CA1789668006
Gene: CYP7B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.64624434T= , CM000670.2:g.64624434T= GRCh38
NC_000008.10:g.65536991T= , CM000670.1:g.65536991T= GRCh37
NC_000008.9:g.65699545T= NCBI36
NG_008338.1:g.179358A=
NG_008338.2:g.179358A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000310193.4:c.228A= MANE Select ENSP00000310721.3:p.Gln76=
ENST00000310193.3:c.228A= ENSP00000310721.3:p.Gln76=
NM_004820.3:c.228A= NP_004811.1:p.Gln76=
NM_001324112.1:c.228A= NP_001311041.1:p.Gln76=
NM_004820.4:c.228A= NP_004811.1:p.Gln76=
XM_017014002.1:c.294A= XP_016869491.1:p.Gln98=
NM_004820.5:c.228A= MANE Select NP_004811.1:p.Gln76=
NM_001324112.2:c.228A= NP_001311041.1:p.Gln76=