Canonical Allele Identifier: CA385501079
Gene: CYP27B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57763726C>G , CM000674.2:g.57763726C>G GRCh38
NC_000012.11:g.58157509C>G , CM000674.1:g.58157509C>G GRCh37
NC_000012.10:g.56443776C>G NCBI36
NG_007076.1:g.8468G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000713544.1:c.1379G>C ENSP00000518840.1:p.Trp460Ser
ENST00000713545.1:c.*303G>C ENSP00000518841.1:n.*303G>C
ENST00000228606.9:c.1298G>C MANE Select ENSP00000228606.4:p.Trp433Ser
ENST00000228606.8:c.1298G>C ENSP00000228606.4:p.Trp433Ser
ENST00000547344.5:n.1437G>C
NM_000785.3:c.1298G>C NP_000776.1:p.Trp433Ser
NM_000785.4:c.1298G>C MANE Select NP_000776.1:p.Trp433Ser