Canonical Allele Identifier: CA371338664
Gene: CYP7B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.64624476T>A , CM000670.2:g.64624476T>A GRCh38
NC_000008.10:g.65537033T>A , CM000670.1:g.65537033T>A GRCh37
NC_000008.9:g.65699587T>A NCBI36
NG_008338.1:g.179316A>T
NG_008338.2:g.179316A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000310193.4:c.186A>T MANE Select ENSP00000310721.3:p.Leu62Phe
ENST00000310193.3:c.186A>T ENSP00000310721.3:p.Leu62Phe
NM_004820.3:c.186A>T NP_004811.1:p.Leu62Phe
NM_001324112.1:c.186A>T NP_001311041.1:p.Leu62Phe
NM_004820.4:c.186A>T NP_004811.1:p.Leu62Phe
XM_017014002.1:c.252A>T XP_016869491.1:p.Leu84Phe
NM_004820.5:c.186A>T MANE Select NP_004811.1:p.Leu62Phe
NM_001324112.2:c.186A>T NP_001311041.1:p.Leu62Phe