Canonical Allele Identifier: CA385505112
Gene: CYP27B1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.58158793C>G (hg19) chr12:g.57765010C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57765010C>G , CM000674.2:g.57765010C>G GRCh38
NC_000012.11:g.58158793C>G , CM000674.1:g.58158793C>G GRCh37
NC_000012.10:g.56445060C>G NCBI36
NG_007076.1:g.7184G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000713544.1:c.871+1G>C ENSP00000518840.1:n.871+1G>C
ENST00000713545.1:c.848+1G>C ENSP00000518841.1:n.848+1G>C
ENST00000228606.9:c.790+1G>C MANE Select ENSP00000228606.4:n.790+1G>C
ENST00000228606.8:c.790+1G>C ENSP00000228606.4:n.790+1G>C
ENST00000546567.5:c.85+1G>C ENSP00000449472.1:n.85+1G>C
ENST00000547344.5:n.929+1G>C
ENST00000547451.1:n.590+1G>C
NM_000785.3:c.790+1G>C NP_000776.1:n.790+1G>C
NM_000785.4:c.790+1G>C MANE Select NP_000776.1:n.790+1G>C
Search 100 bp 5'
Search 100 bp 3'