Canonical Allele Identifier: CA2619519150

Gene: CYP27B1

Linked Data

• gnomAD v4: 12-57765987-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57765992del , CM000674.2:g.57765992del	GRCh38
NC_000012.11:g.58159775del , CM000674.1:g.58159775del	GRCh37
NC_000012.10:g.56446042del	NCBI36
NG_007076.1:g.6206del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000546609.2:n.298+19del
ENST00000713544.1:c.386+19del	ENSP00000518840.1:n.386+19del
ENST00000713545.1:c.386+19del	ENSP00000518841.1:n.386+19del
ENST00000228606.9:c.386+19del MANE Select	ENSP00000228606.4:n.386+19del
ENST00000228606.8:c.386+19del	ENSP00000228606.4:n.386+19del
ENST00000546496.1:n.214+19del
ENST00000546609.1:c.298+19del
ENST00000547344.5:n.440+19del
ENST00000552186.1:n.505+19del
NM_000785.3:c.386+19del	NP_000776.1:n.386+19del
NM_000785.4:c.386+19del MANE Select	NP_000776.1:n.386+19del