Canonical Allele Identifier: CA2038987701
Gene: CYP27B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57764536G= , CM000674.2:g.57764536G= GRCh38
NC_000012.11:g.58158319G= , CM000674.1:g.58158319G= GRCh37
NC_000012.10:g.56444586G= NCBI36
NG_007076.1:g.7658C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000713544.1:c.1059C= ENSP00000518840.1:p.Leu353=
ENST00000713545.1:c.1036C= ENSP00000518841.1:p.Leu346=
ENST00000228606.9:c.978C= MANE Select ENSP00000228606.4:p.Leu326=
ENST00000228606.8:c.978C= ENSP00000228606.4:p.Leu326=
ENST00000546567.5:c.273C= ENSP00000449472.1:p.Leu91=
ENST00000547344.5:n.1117C=
NM_000785.3:c.978C= NP_000776.1:p.Leu326=
NM_000785.4:c.978C= MANE Select NP_000776.1:p.Leu326=