Canonical Allele Identifier: CA690329471
Gene: CYP27B1 HGNC NCBI

Linked Data

dbSNP Id: rs1193100358

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57764094T>C , CM000674.2:g.57764094T>C GRCh38
NC_000012.11:g.58157877T>C , CM000674.1:g.58157877T>C GRCh37
NC_000012.10:g.56444144T>C NCBI36
NG_007076.1:g.8100A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000713544.1:c.1296+4A>G ENSP00000518840.1:n.1296+4A>G
ENST00000713545.1:c.*220+4A>G ENSP00000518841.1:n.*220+4A>G
ENST00000228606.9:c.1215+4A>G MANE Select ENSP00000228606.4:n.1215+4A>G
ENST00000228606.8:c.1215+4A>G ENSP00000228606.4:n.1215+4A>G
ENST00000547344.5:n.1354+4A>G
NM_000785.3:c.1215+4A>G NP_000776.1:n.1215+4A>G
NM_000785.4:c.1215+4A>G MANE Select NP_000776.1:n.1215+4A>G