Canonical Allele Identifier: CA6658245
Gene: CYP27B1 HGNC NCBI

Linked Data

dbSNP Id: rs745757851

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57764511G>A , CM000674.2:g.57764511G>A GRCh38
NC_000012.11:g.58158294G>A , CM000674.1:g.58158294G>A GRCh37
NC_000012.10:g.56444561G>A NCBI36
NG_007076.1:g.7683C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000713544.1:c.1084C>T ENSP00000518840.1:p.Arg362Trp
ENST00000713545.1:c.*8C>T ENSP00000518841.1:n.*8C>T
ENST00000228606.9:c.1003C>T MANE Select ENSP00000228606.4:p.Arg335Trp
ENST00000228606.8:c.1003C>T ENSP00000228606.4:p.Arg335Trp
ENST00000546567.5:c.298C>T ENSP00000449472.1:p.Arg100Trp
ENST00000547344.5:n.1142C>T
NM_000785.3:c.1003C>T NP_000776.1:p.Arg335Trp
NM_000785.4:c.1003C>T MANE Select NP_000776.1:p.Arg335Trp