Canonical Allele Identifier: CA690331841

Gene: CYP27B1

Linked Data

• dbSNP Id: rs1174531310
• gnomAD v4: 12-57765970-C-A
• MyVariant Identifiers: chr12:g.58159753C>A (hg19) ; chr12:g.57765970C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57765970C>A , CM000674.2:g.57765970C>A	GRCh38
NC_000012.11:g.58159753C>A , CM000674.1:g.58159753C>A	GRCh37
NC_000012.10:g.56446020C>A	NCBI36
NG_007076.1:g.6224G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000546609.2:n.298+37G>T
ENST00000713544.1:c.386+37G>T	ENSP00000518840.1:n.386+37G>T
ENST00000713545.1:c.386+37G>T	ENSP00000518841.1:n.386+37G>T
ENST00000228606.9:c.386+37G>T MANE Select	ENSP00000228606.4:n.386+37G>T
ENST00000228606.8:c.386+37G>T	ENSP00000228606.4:n.386+37G>T
ENST00000546496.1:n.214+37G>T
ENST00000546609.1:c.298+37G>T
ENST00000547344.5:n.440+37G>T
ENST00000552186.1:n.505+37G>T
NM_000785.3:c.386+37G>T	NP_000776.1:n.386+37G>T
NM_000785.4:c.386+37G>T MANE Select	NP_000776.1:n.386+37G>T