Canonical Allele Identifier: CA371338999
Gene: CYP7B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.64624527C>A , CM000670.2:g.64624527C>A GRCh38
NC_000008.10:g.65537084C>A , CM000670.1:g.65537084C>A GRCh37
NC_000008.9:g.65699638C>A NCBI36
NG_008338.1:g.179265G>T
NG_008338.2:g.179265G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000310193.4:c.135G>T MANE Select ENSP00000310721.3:p.Glu45Asp
ENST00000310193.3:c.135G>T ENSP00000310721.3:p.Glu45Asp
NM_004820.3:c.135G>T NP_004811.1:p.Glu45Asp
NM_001324112.1:c.135G>T NP_001311041.1:p.Glu45Asp
NM_004820.4:c.135G>T NP_004811.1:p.Glu45Asp
XM_017014002.1:c.201G>T XP_016869491.1:p.Glu67Asp
NM_004820.5:c.135G>T MANE Select NP_004811.1:p.Glu45Asp
NM_001324112.2:c.135G>T NP_001311041.1:p.Glu45Asp