Canonical Allele Identifier: CA1789667928
Gene: CYP7B1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.64624220T= , CM000670.2:g.64624220T= GRCh38
NC_000008.10:g.65536777T= , CM000670.1:g.65536777T= GRCh37
NC_000008.9:g.65699331T= NCBI36
NG_008338.1:g.179572A=
NG_008338.2:g.179572A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000310193.4:c.259+183A= MANE Select ENSP00000310721.3:n.259+183A=
ENST00000310193.3:c.259+183A= ENSP00000310721.3:n.259+183A=
NM_004820.3:c.259+183A= NP_004811.1:n.259+183A=
NM_001324112.1:c.259+183A= NP_001311041.1:n.259+183A=
NM_004820.4:c.259+183A= NP_004811.1:n.259+183A=
XM_017014002.1:c.325+183A= XP_016869491.1:n.325+183A=
NM_004820.5:c.259+183A= MANE Select NP_004811.1:n.259+183A=
NM_001324112.2:c.259+183A= NP_001311041.1:n.259+183A=
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