Canonical Allele Identifier: CA6658386
Gene: CYP27B1 HGNC NCBI

Linked Data

dbSNP Id: rs751768889
ExAC: 12:58159011 G / T
gnomAD v2: 12-58159011-G-T
gnomAD v3: 12-57765228-G-T
gnomAD v4: 12-57765228-G-T
MyVariant Identifiers: chr12:g.58159011G>T (hg19) chr12:g.57765228G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57765228G>T , CM000674.2:g.57765228G>T GRCh38
NC_000012.11:g.58159011G>T , CM000674.1:g.58159011G>T GRCh37
NC_000012.10:g.56445278G>T NCBI36
NG_007076.1:g.6966C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000546609.2:n.502-17C>A
ENST00000713544.1:c.671-17C>A ENSP00000518840.1:n.671-17C>A
ENST00000713545.1:c.648-17C>A ENSP00000518841.1:n.648-17C>A
ENST00000228606.9:c.590-17C>A MANE Select ENSP00000228606.4:n.590-17C>A
ENST00000228606.8:c.590-17C>A ENSP00000228606.4:n.590-17C>A
ENST00000546567.5:c.-116-17C>A ENSP00000449472.1:n.-116-17C>A
ENST00000546609.1:c.502-17C>A
ENST00000547344.5:n.712C>A
ENST00000547451.1:n.390-17C>A
NM_000785.3:c.590-17C>A NP_000776.1:n.590-17C>A
NM_000785.4:c.590-17C>A MANE Select NP_000776.1:n.590-17C>A
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