Canonical Allele Identifier: CA480269376

Gene: CYP27B1

Linked Data

• gnomAD v4: 12-57766027-C-A
• MyVariant Identifiers: chr12:g.58159810C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57766027C>A , CM000674.2:g.57766027C>A	GRCh38
NC_000012.11:g.58159810C>A , CM000674.1:g.58159810C>A	GRCh37
NC_000012.10:g.56446077C>A	NCBI36
NG_007076.1:g.6167G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000546609.2:n.278G>T
ENST00000713544.1:c.366G>T	ENSP00000518840.1:p.Arg122=
ENST00000713545.1:c.366G>T	ENSP00000518841.1:p.Arg122=
ENST00000228606.9:c.366G>T MANE Select	ENSP00000228606.4:p.Arg122=
ENST00000228606.8:c.366G>T	ENSP00000228606.4:p.Arg122=
ENST00000546496.1:n.194G>T
ENST00000546609.1:c.278G>T
ENST00000547344.5:n.420G>T
ENST00000552186.1:n.485G>T
NM_000785.3:c.366G>T	NP_000776.1:p.Arg122=
NM_000785.4:c.366G>T MANE Select	NP_000776.1:p.Arg122=