Canonical Allele Identifier: CA385501220
Gene: CYP27B1 HGNC NCBI

Linked Data

gnomAD v4: 12-57763790-G-T
MyVariant Identifiers: chr12:g.58157573G>T (hg19) chr12:g.57763790G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57763790G>T , CM000674.2:g.57763790G>T GRCh38
NC_000012.11:g.58157573G>T , CM000674.1:g.58157573G>T GRCh37
NC_000012.10:g.56443840G>T NCBI36
NG_007076.1:g.8404C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000713544.1:c.1315C>A ENSP00000518840.1:p.His439Asn
ENST00000713545.1:c.*239C>A ENSP00000518841.1:n.*239C>A
ENST00000228606.9:c.1234C>A MANE Select ENSP00000228606.4:p.His412Asn
ENST00000228606.8:c.1234C>A ENSP00000228606.4:p.His412Asn
ENST00000547344.5:n.1373C>A
NM_000785.3:c.1234C>A NP_000776.1:p.His412Asn
NM_000785.4:c.1234C>A MANE Select NP_000776.1:p.His412Asn
Search 100 bp 5'
Search 100 bp 3'