Canonical Allele Identifier: CA2796149717
Gene: CYP27B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57765229C>A , CM000674.2:g.57765229C>A GRCh38
NC_000012.11:g.58159012C>A , CM000674.1:g.58159012C>A GRCh37
NC_000012.10:g.56445279C>A NCBI36
NG_007076.1:g.6965G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000546609.2:n.502-18G>T
ENST00000713544.1:c.671-18G>T ENSP00000518840.1:n.671-18G>T
ENST00000713545.1:c.648-18G>T ENSP00000518841.1:n.648-18G>T
ENST00000228606.9:c.590-18G>T MANE Select ENSP00000228606.4:n.590-18G>T
ENST00000228606.8:c.590-18G>T ENSP00000228606.4:n.590-18G>T
ENST00000546567.5:c.-116-18G>T ENSP00000449472.1:n.-116-18G>T
ENST00000546609.1:c.502-18G>T
ENST00000547344.5:n.711G>T
ENST00000547451.1:n.390-18G>T
NM_000785.3:c.590-18G>T NP_000776.1:n.590-18G>T
NM_000785.4:c.590-18G>T MANE Select NP_000776.1:n.590-18G>T