Canonical Allele Identifier: CA385503357

Gene: CYP27B1

Linked Data

• dbSNP Id: rs1955341535
• gnomAD v3: 12-57764411-G-T
• gnomAD v4: 12-57764411-G-T
• MyVariant Identifiers: chr12:g.58158194G>T (hg19) ; chr12:g.57764411G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57764411G>T , CM000674.2:g.57764411G>T	GRCh38
NC_000012.11:g.58158194G>T , CM000674.1:g.58158194G>T	GRCh37
NC_000012.10:g.56444461G>T	NCBI36
NG_007076.1:g.7783C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000713544.1:c.1184C>A	ENSP00000518840.1:p.Pro395His
ENST00000713545.1:c.*108C>A	ENSP00000518841.1:n.*108C>A
ENST00000228606.9:c.1103C>A MANE Select	ENSP00000228606.4:p.Pro368His
ENST00000228606.8:c.1103C>A	ENSP00000228606.4:p.Pro368His
ENST00000546567.5:c.398C>A	ENSP00000449472.1:p.Pro133His
ENST00000547344.5:n.1242C>A
NM_000785.3:c.1103C>A	NP_000776.1:p.Pro368His
NM_000785.4:c.1103C>A MANE Select	NP_000776.1:p.Pro368His