Canonical Allele Identifier: CA690331734

Gene: CYP27B1

Linked Data

• dbSNP Id: rs1445542658
• gnomAD v3: 12-57765767-T-C
• gnomAD v4: 12-57765767-T-C
• MyVariant Identifiers: chr12:g.58159550T>C (hg19) ; chr12:g.57765767T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57765767T>C , CM000674.2:g.57765767T>C	GRCh38
NC_000012.11:g.58159550T>C , CM000674.1:g.58159550T>C	GRCh37
NC_000012.10:g.56445817T>C	NCBI36
NG_007076.1:g.6427A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000546609.2:n.298+240A>G
ENST00000713544.1:c.387-187A>G	ENSP00000518840.1:n.387-187A>G
ENST00000713545.1:c.387-210A>G	ENSP00000518841.1:n.387-210A>G
ENST00000228606.9:c.386+240A>G MANE Select	ENSP00000228606.4:n.386+240A>G
ENST00000228606.8:c.386+240A>G	ENSP00000228606.4:n.386+240A>G
ENST00000546496.1:n.214+240A>G
ENST00000546609.1:c.298+240A>G
ENST00000547344.5:n.440+240A>G
ENST00000552186.1:n.505+240A>G
NM_000785.3:c.386+240A>G	NP_000776.1:n.386+240A>G
NM_000785.4:c.386+240A>G MANE Select	NP_000776.1:n.386+240A>G