Canonical Allele Identifier: CA385502588
Gene: CYP27B1 HGNC NCBI

Linked Data

dbSNP Id: rs1595117628

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57764135T>C , CM000674.2:g.57764135T>C GRCh38
NC_000012.11:g.58157918T>C , CM000674.1:g.58157918T>C GRCh37
NC_000012.10:g.56444185T>C NCBI36
NG_007076.1:g.8059A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000713544.1:c.1259A>G ENSP00000518840.1:p.Lys420Arg
ENST00000713545.1:c.*183A>G ENSP00000518841.1:n.*183A>G
ENST00000228606.9:c.1178A>G MANE Select ENSP00000228606.4:p.Lys393Arg
ENST00000228606.8:c.1178A>G ENSP00000228606.4:p.Lys393Arg
ENST00000547344.5:n.1317A>G
NM_000785.3:c.1178A>G NP_000776.1:p.Lys393Arg
NM_000785.4:c.1178A>G MANE Select NP_000776.1:p.Lys393Arg