Canonical Allele Identifier: CA2038987185
Gene: CYP27B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57764181G= , CM000674.2:g.57764181G= GRCh38
NC_000012.11:g.58157964G= , CM000674.1:g.58157964G= GRCh37
NC_000012.10:g.56444231G= NCBI36
NG_007076.1:g.8013C=

Transcript Alleles

HGVS Amino-acid change
ENST00000713544.1:c.1218-5C= ENSP00000518840.1:n.1218-5C=
ENST00000713545.1:c.*142-5C= ENSP00000518841.1:n.*142-5C=
ENST00000228606.9:c.1137-5C= MANE Select ENSP00000228606.4:n.1137-5C=
ENST00000228606.8:c.1137-5C= ENSP00000228606.4:n.1137-5C=
ENST00000546567.5:c.432-5C= ENSP00000449472.1:n.432-5C=
ENST00000547344.5:n.1276-5C=
NM_000785.3:c.1137-5C= NP_000776.1:n.1137-5C=
NM_000785.4:c.1137-5C= MANE Select NP_000776.1:n.1137-5C=