Canonical Allele Identifier: CA2038987872
Gene: CYP27B1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57764656A= , CM000674.2:g.57764656A= GRCh38
NC_000012.11:g.58158439A= , CM000674.1:g.58158439A= GRCh37
NC_000012.10:g.56444706A= NCBI36
NG_007076.1:g.7538T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000713544.1:c.1044+98T= ENSP00000518840.1:n.1044+98T=
ENST00000713545.1:c.1021+98T= ENSP00000518841.1:n.1021+98T=
ENST00000228606.9:c.963+98T= MANE Select ENSP00000228606.4:n.963+98T=
ENST00000228606.8:c.963+98T= ENSP00000228606.4:n.963+98T=
ENST00000546567.5:c.258+98T= ENSP00000449472.1:n.258+98T=
ENST00000547344.5:n.1102+98T=
ENST00000547451.1:n.861T=
NM_000785.3:c.963+98T= NP_000776.1:n.963+98T=
NM_000785.4:c.963+98T= MANE Select NP_000776.1:n.963+98T=
Search 100 bp 5'
Search 100 bp 3'