Canonical Allele Identifier: CA2687454815
Gene: CYP7B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.64624339_64624342del , CM000670.2:g.64624339_64624342del GRCh38
NC_000008.10:g.65536896_65536899del , CM000670.1:g.65536896_65536899del GRCh37
NC_000008.9:g.65699450_65699453del NCBI36
NG_008338.1:g.179453_179456del
NG_008338.2:g.179453_179456del

Transcript Alleles

HGVS Amino-acid Change
ENST00000310193.4:c.259+64_259+67del MANE Select ENSP00000310721.3:n.259+64_259+67del
ENST00000310193.3:c.259+64_259+67del ENSP00000310721.3:n.259+64_259+67del
NM_004820.3:c.259+64_259+67del NP_004811.1:n.259+64_259+67del
NM_001324112.1:c.259+64_259+67del NP_001311041.1:n.259+64_259+67del
NM_004820.4:c.259+64_259+67del NP_004811.1:n.259+64_259+67del
XM_017014002.1:c.325+64_325+67del XP_016869491.1:n.325+64_325+67del
NM_004820.5:c.259+64_259+67del MANE Select NP_004811.1:n.259+64_259+67del
NM_001324112.2:c.259+64_259+67del NP_001311041.1:n.259+64_259+67del