Canonical Allele Identifier: CA385503470

Gene: CYP27B1

Linked Data

• MyVariant Identifiers: chr12:g.58158215G>A (hg19) ; chr12:g.57764432G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57764432G>A , CM000674.2:g.57764432G>A	GRCh38
NC_000012.11:g.58158215G>A , CM000674.1:g.58158215G>A	GRCh37
NC_000012.10:g.56444482G>A	NCBI36
NG_007076.1:g.7762C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000713544.1:c.1163C>T	ENSP00000518840.1:p.Ala388Val
ENST00000713545.1:c.*87C>T	ENSP00000518841.1:n.*87C>T
ENST00000228606.9:c.1082C>T MANE Select	ENSP00000228606.4:p.Ala361Val
ENST00000228606.8:c.1082C>T	ENSP00000228606.4:p.Ala361Val
ENST00000546567.5:c.377C>T	ENSP00000449472.1:p.Ala126Val
ENST00000547344.5:n.1221C>T
NM_000785.3:c.1082C>T	NP_000776.1:p.Ala361Val
NM_000785.4:c.1082C>T MANE Select	NP_000776.1:p.Ala361Val