Canonical Allele Identifier: CA480269570
Gene: CYP27B1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.58159909A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57766126A>C , CM000674.2:g.57766126A>C GRCh38
NC_000012.11:g.58159909A>C , CM000674.1:g.58159909A>C GRCh37
NC_000012.10:g.56446176A>C NCBI36
NG_007076.1:g.6068T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000546609.2:n.179T>G
ENST00000713544.1:c.267T>G ENSP00000518840.1:p.Ala89=
ENST00000713545.1:c.267T>G ENSP00000518841.1:p.Ala89=
ENST00000228606.9:c.267T>G MANE Select ENSP00000228606.4:p.Ala89=
ENST00000228606.8:c.267T>G ENSP00000228606.4:p.Ala89=
ENST00000546496.1:n.95T>G
ENST00000546609.1:c.179T>G
ENST00000547344.5:n.321T>G
ENST00000552186.1:n.386T>G
NM_000785.3:c.267T>G NP_000776.1:p.Ala89=
NM_000785.4:c.267T>G MANE Select NP_000776.1:p.Ala89=
Search 100 bp 5'
Search 100 bp 3'