Canonical Allele Identifier: CA480401647
Gene: CYP27B1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.58158214G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57764431G>T , CM000674.2:g.57764431G>T GRCh38
NC_000012.11:g.58158214G>T , CM000674.1:g.58158214G>T GRCh37
NC_000012.10:g.56444481G>T NCBI36
NG_007076.1:g.7763C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000713544.1:c.1164C>A ENSP00000518840.1:p.Ala388=
ENST00000713545.1:c.*88C>A ENSP00000518841.1:n.*88C>A
ENST00000228606.9:c.1083C>A MANE Select ENSP00000228606.4:p.Ala361=
ENST00000228606.8:c.1083C>A ENSP00000228606.4:p.Ala361=
ENST00000546567.5:c.378C>A ENSP00000449472.1:p.Ala126=
ENST00000547344.5:n.1222C>A
NM_000785.3:c.1083C>A NP_000776.1:p.Ala361=
NM_000785.4:c.1083C>A MANE Select NP_000776.1:p.Ala361=