Canonical Allele Identifier: CA2737087939

Gene: CYP24A1

Linked Data

• dbSNP Id: rs2146502168

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.54169585A>G , CM000682.2:g.54169585A>G	GRCh38
NC_000020.10:g.52786124A>G , CM000682.1:g.52786124A>G	GRCh37
NC_000020.9:g.52219531A>G	NCBI36
NG_008334.1:g.9393T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000216862.8:c.640+7T>C MANE Select	ENSP00000216862.3:n.640+7T>C
ENST00000216862.7:c.640+7T>C	ENSP00000216862.3:n.640+7T>C
ENST00000395954.3:c.214+7T>C	ENSP00000379284.3:n.214+7T>C
ENST00000395955.7:c.640+7T>C	ENSP00000379285.3:n.640+7T>C
NM_000782.4:c.640+7T>C	NP_000773.2:n.640+7T>C
NM_001128915.1:c.640+7T>C	NP_001122387.1:n.640+7T>C
XM_005260304.3:c.640+7T>C	XP_005260361.1:n.640+7T>C
XM_005260304.5:c.640+7T>C	XP_005260361.1:n.640+7T>C
XM_017027691.2:c.640+7T>C	XP_016883180.1:n.640+7T>C
XM_017027692.2:c.640+7T>C	XP_016883181.1:n.640+7T>C
XM_017027693.2:c.640+7T>C	XP_016883182.1:n.640+7T>C
NM_000782.5:c.640+7T>C MANE Select	NP_000773.2:n.640+7T>C
NM_001128915.2:c.640+7T>C	NP_001122387.1:n.640+7T>C