Canonical Allele Identifier: CA2039015995
Gene: CYP27B1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57764043G= , CM000674.2:g.57764043G= GRCh38
NC_000012.11:g.58157826G= , CM000674.1:g.58157826G= GRCh37
NC_000012.10:g.56444093G= NCBI36
NG_007076.1:g.8151C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000713544.1:c.1296+55C= ENSP00000518840.1:n.1296+55C=
ENST00000713545.1:c.*220+55C= ENSP00000518841.1:n.*220+55C=
ENST00000228606.9:c.1215+55C= MANE Select ENSP00000228606.4:n.1215+55C=
ENST00000228606.8:c.1215+55C= ENSP00000228606.4:n.1215+55C=
ENST00000547344.5:n.1354+55C=
NM_000785.3:c.1215+55C= NP_000776.1:n.1215+55C=
NM_000785.4:c.1215+55C= MANE Select NP_000776.1:n.1215+55C=
Search 100 bp 5'
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