Canonical Allele Identifier: CA2619516112

Gene: CYP27B1

Linked Data

• gnomAD v4: 12-57764563-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57764564dup , CM000674.2:g.57764564dup	GRCh38
NC_000012.11:g.58158347dup , CM000674.1:g.58158347dup	GRCh37
NC_000012.10:g.56444614dup	NCBI36
NG_007076.1:g.7630dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000713544.1:c.1045-14dup	ENSP00000518840.1:n.1045-14dup
ENST00000713545.1:c.1022-14dup	ENSP00000518841.1:n.1022-14dup
ENST00000228606.9:c.964-14dup MANE Select	ENSP00000228606.4:n.964-14dup
ENST00000228606.8:c.964-14dup	ENSP00000228606.4:n.964-14dup
ENST00000546567.5:c.259-14dup	ENSP00000449472.1:n.259-14dup
ENST00000547344.5:n.1103-14dup
ENST00000547451.1:n.953dup
NM_000785.3:c.964-14dup	NP_000776.1:n.964-14dup
NM_000785.4:c.964-14dup MANE Select	NP_000776.1:n.964-14dup