Canonical Allele Identifier: CA2038987253
Gene: CYP27B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57764229C= , CM000674.2:g.57764229C= GRCh38
NC_000012.11:g.58158012C= , CM000674.1:g.58158012C= GRCh37
NC_000012.10:g.56444279C= NCBI36
NG_007076.1:g.7965G=

Transcript Alleles

HGVS Amino-acid change
ENST00000713544.1:c.1218-53G= ENSP00000518840.1:n.1218-53G=
ENST00000713545.1:c.*142-53G= ENSP00000518841.1:n.*142-53G=
ENST00000228606.9:c.1137-53G= MANE Select ENSP00000228606.4:n.1137-53G=
ENST00000228606.8:c.1137-53G= ENSP00000228606.4:n.1137-53G=
ENST00000546567.5:c.432-53G= ENSP00000449472.1:n.432-53G=
ENST00000547344.5:n.1276-53G=
NM_000785.3:c.1137-53G= NP_000776.1:n.1137-53G=
NM_000785.4:c.1137-53G= MANE Select NP_000776.1:n.1137-53G=