Canonical Allele Identifier: CA2038990293

Gene: CYP27B1

Linked Data

• dbSNP Id: rs1955355577
• gnomAD v4: 12-57765825-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57765825G>A , CM000674.2:g.57765825G>A	GRCh38
NC_000012.11:g.58159608G>A , CM000674.1:g.58159608G>A	GRCh37
NC_000012.10:g.56445875G>A	NCBI36
NG_007076.1:g.6369C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000546609.2:n.298+182C>T
ENST00000713544.1:c.386+182C>T	ENSP00000518840.1:n.386+182C>T
ENST00000713545.1:c.386+182C>T	ENSP00000518841.1:n.386+182C>T
ENST00000228606.9:c.386+182C>T MANE Select	ENSP00000228606.4:n.386+182C>T
ENST00000228606.8:c.386+182C>T	ENSP00000228606.4:n.386+182C>T
ENST00000546496.1:n.214+182C>T
ENST00000546609.1:c.298+182C>T
ENST00000547344.5:n.440+182C>T
ENST00000552186.1:n.505+182C>T
NM_000785.3:c.386+182C>T	NP_000776.1:n.386+182C>T
NM_000785.4:c.386+182C>T MANE Select	NP_000776.1:n.386+182C>T