Canonical Allele Identifier: CA2038987769
Gene: CYP27B1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57764593C= , CM000674.2:g.57764593C= GRCh38
NC_000012.11:g.58158376C= , CM000674.1:g.58158376C= GRCh37
NC_000012.10:g.56444643C= NCBI36
NG_007076.1:g.7601G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000713544.1:c.1045-43G= ENSP00000518840.1:n.1045-43G=
ENST00000713545.1:c.1022-43G= ENSP00000518841.1:n.1022-43G=
ENST00000228606.9:c.964-43G= MANE Select ENSP00000228606.4:n.964-43G=
ENST00000228606.8:c.964-43G= ENSP00000228606.4:n.964-43G=
ENST00000546567.5:c.259-43G= ENSP00000449472.1:n.259-43G=
ENST00000547344.5:n.1103-43G=
ENST00000547451.1:n.924G=
NM_000785.3:c.964-43G= NP_000776.1:n.964-43G=
NM_000785.4:c.964-43G= MANE Select NP_000776.1:n.964-43G=
Search 100 bp 5'
Search 100 bp 3'