Canonical Allele Identifier: CA371338835
Gene: CYP7B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.64624499A>T , CM000670.2:g.64624499A>T GRCh38
NC_000008.10:g.65537056A>T , CM000670.1:g.65537056A>T GRCh37
NC_000008.9:g.65699610A>T NCBI36
NG_008338.1:g.179293T>A
NG_008338.2:g.179293T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000310193.4:c.163T>A MANE Select ENSP00000310721.3:p.Tyr55Asn
ENST00000310193.3:c.163T>A ENSP00000310721.3:p.Tyr55Asn
NM_004820.3:c.163T>A NP_004811.1:p.Tyr55Asn
NM_001324112.1:c.163T>A NP_001311041.1:p.Tyr55Asn
NM_004820.4:c.163T>A NP_004811.1:p.Tyr55Asn
XM_017014002.1:c.229T>A XP_016869491.1:p.Tyr77Asn
NM_004820.5:c.163T>A MANE Select NP_004811.1:p.Tyr55Asn
NM_001324112.2:c.163T>A NP_001311041.1:p.Tyr55Asn