Canonical Allele Identifier: CA480269230
Gene: CYP27B1 HGNC NCBI

Linked Data

dbSNP Id: rs1235706462
MyVariant Identifiers: chr12:g.58157460G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57763677G>C , CM000674.2:g.57763677G>C GRCh38
NC_000012.11:g.58157460G>C , CM000674.1:g.58157460G>C GRCh37
NC_000012.10:g.56443727G>C NCBI36
NG_007076.1:g.8517C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000713544.1:c.1428C>G ENSP00000518840.1:p.Gly476=
ENST00000713545.1:c.*352C>G ENSP00000518841.1:n.*352C>G
ENST00000228606.9:c.1347C>G MANE Select ENSP00000228606.4:p.Gly449=
ENST00000228606.8:c.1347C>G ENSP00000228606.4:p.Gly449=
ENST00000547344.5:n.1486C>G
NM_000785.3:c.1347C>G NP_000776.1:p.Gly449=
NM_000785.4:c.1347C>G MANE Select NP_000776.1:p.Gly449=
Search 100 bp 5'
Search 100 bp 3'