Canonical Allele Identifier: CA1789667976
Gene: CYP7B1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.64624356G= , CM000670.2:g.64624356G= GRCh38
NC_000008.10:g.65536913G= , CM000670.1:g.65536913G= GRCh37
NC_000008.9:g.65699467G= NCBI36
NG_008338.1:g.179436C=
NG_008338.2:g.179436C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000310193.4:c.259+47C= MANE Select ENSP00000310721.3:n.259+47C=
ENST00000310193.3:c.259+47C= ENSP00000310721.3:n.259+47C=
NM_004820.3:c.259+47C= NP_004811.1:n.259+47C=
NM_001324112.1:c.259+47C= NP_001311041.1:n.259+47C=
NM_004820.4:c.259+47C= NP_004811.1:n.259+47C=
XM_017014002.1:c.325+47C= XP_016869491.1:n.325+47C=
NM_004820.5:c.259+47C= MANE Select NP_004811.1:n.259+47C=
NM_001324112.2:c.259+47C= NP_001311041.1:n.259+47C=
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