Canonical Allele Identifier: CA2038987864
Gene: CYP27B1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57764649C= , CM000674.2:g.57764649C= GRCh38
NC_000012.11:g.58158432C= , CM000674.1:g.58158432C= GRCh37
NC_000012.10:g.56444699C= NCBI36
NG_007076.1:g.7545G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000713544.1:c.1045-99G= ENSP00000518840.1:n.1045-99G=
ENST00000713545.1:c.1022-99G= ENSP00000518841.1:n.1022-99G=
ENST00000228606.9:c.964-99G= MANE Select ENSP00000228606.4:n.964-99G=
ENST00000228606.8:c.964-99G= ENSP00000228606.4:n.964-99G=
ENST00000546567.5:c.259-99G= ENSP00000449472.1:n.259-99G=
ENST00000547344.5:n.1103-99G=
ENST00000547451.1:n.868G=
NM_000785.3:c.964-99G= NP_000776.1:n.964-99G=
NM_000785.4:c.964-99G= MANE Select NP_000776.1:n.964-99G=
Search 100 bp 5'
Search 100 bp 3'