Canonical Allele Identifier: CA480401851
Gene: CYP27B1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.58158309G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57764526G>A , CM000674.2:g.57764526G>A GRCh38
NC_000012.11:g.58158309G>A , CM000674.1:g.58158309G>A GRCh37
NC_000012.10:g.56444576G>A NCBI36
NG_007076.1:g.7668C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000713544.1:c.1069C>T ENSP00000518840.1:p.Leu357=
ENST00000713545.1:c.1046C>T ENSP00000518841.1:p.Ser349Phe
ENST00000228606.9:c.988C>T MANE Select ENSP00000228606.4:p.Leu330=
ENST00000228606.8:c.988C>T ENSP00000228606.4:p.Leu330=
ENST00000546567.5:c.283C>T ENSP00000449472.1:p.Leu95=
ENST00000547344.5:n.1127C>T
NM_000785.3:c.988C>T NP_000776.1:p.Leu330=
NM_000785.4:c.988C>T MANE Select NP_000776.1:p.Leu330=