Canonical Allele Identifier: CA237814095
Gene: CYP27B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3023914
ClinVar RCV Id: RCV003881009
dbSNP Id: rs908451945
gnomAD v2: 12-58158143-C-T
gnomAD v4: 12-57764360-C-T
MyVariant Identifiers: chr12:g.58158143C>T (hg19) chr12:g.57764360C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57764360C>T , CM000674.2:g.57764360C>T GRCh38
NC_000012.11:g.58158143C>T , CM000674.1:g.58158143C>T GRCh37
NC_000012.10:g.56444410C>T NCBI36
NG_007076.1:g.7834G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000713544.1:c.1217+18G>A ENSP00000518840.1:n.1217+18G>A
ENST00000713545.1:c.*141+18G>A ENSP00000518841.1:n.*141+18G>A
ENST00000228606.9:c.1136+18G>A MANE Select ENSP00000228606.4:n.1136+18G>A
ENST00000228606.8:c.1136+18G>A ENSP00000228606.4:n.1136+18G>A
ENST00000546567.5:c.431+18G>A ENSP00000449472.1:n.431+18G>A
ENST00000547344.5:n.1275+18G>A
NM_000785.3:c.1136+18G>A NP_000776.1:n.1136+18G>A
NM_000785.4:c.1136+18G>A MANE Select NP_000776.1:n.1136+18G>A
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