Canonical Allele Identifier: CA385507537

Gene: CYP27B1

Linked Data

• gnomAD v4: 12-57766010-G-A
• MyVariant Identifiers: chr12:g.58159793G>A (hg19) ; chr12:g.57766010G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57766010G>A , CM000674.2:g.57766010G>A	GRCh38
NC_000012.11:g.58159793G>A , CM000674.1:g.58159793G>A	GRCh37
NC_000012.10:g.56446060G>A	NCBI36
NG_007076.1:g.6184C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000546609.2:n.295C>T
ENST00000713544.1:c.383C>T	ENSP00000518840.1:p.Thr128Ile
ENST00000713545.1:c.383C>T	ENSP00000518841.1:p.Thr128Ile
ENST00000228606.9:c.383C>T MANE Select	ENSP00000228606.4:p.Thr128Ile
ENST00000228606.8:c.383C>T	ENSP00000228606.4:p.Thr128Ile
ENST00000546496.1:n.211C>T
ENST00000546609.1:c.295C>T
ENST00000547344.5:n.437C>T
ENST00000552186.1:n.502C>T
NM_000785.3:c.383C>T	NP_000776.1:p.Thr128Ile
NM_000785.4:c.383C>T MANE Select	NP_000776.1:p.Thr128Ile