Canonical Allele Identifier: CA2687454869

Gene: CYP7B1

Linked Data

• gnomAD v4: 8-64624559-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.64624559G>T , CM000670.2:g.64624559G>T	GRCh38
NC_000008.10:g.65537116G>T , CM000670.1:g.65537116G>T	GRCh37
NC_000008.9:g.65699670G>T	NCBI36
NG_008338.1:g.179233C>A
NG_008338.2:g.179233C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310193.4:c.123-20C>A MANE Select	ENSP00000310721.3:n.123-20C>A
ENST00000310193.3:c.123-20C>A	ENSP00000310721.3:n.123-20C>A
NM_004820.3:c.123-20C>A	NP_004811.1:n.123-20C>A
NM_001324112.1:c.123-20C>A	NP_001311041.1:n.123-20C>A
NM_004820.4:c.123-20C>A	NP_004811.1:n.123-20C>A
XM_017014002.1:c.189-20C>A	XP_016869491.1:n.189-20C>A
NM_004820.5:c.123-20C>A MANE Select	NP_004811.1:n.123-20C>A
NM_001324112.2:c.123-20C>A	NP_001311041.1:n.123-20C>A