Canonical Allele Identifier: CA2039015567
Gene: CYP27B1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57763799T= , CM000674.2:g.57763799T= GRCh38
NC_000012.11:g.58157582T= , CM000674.1:g.58157582T= GRCh37
NC_000012.10:g.56443849T= NCBI36
NG_007076.1:g.8395A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000713544.1:c.1306A= ENSP00000518840.1:p.Thr436=
ENST00000713545.1:c.*230A= ENSP00000518841.1:n.*230A=
ENST00000228606.9:c.1225A= MANE Select ENSP00000228606.4:p.Thr409=
ENST00000228606.8:c.1225A= ENSP00000228606.4:p.Thr409=
ENST00000547344.5:n.1364A=
NM_000785.3:c.1225A= NP_000776.1:p.Thr409=
NM_000785.4:c.1225A= MANE Select NP_000776.1:p.Thr409=
Search 100 bp 5'
Search 100 bp 3'