Canonical Allele Identifier: CA2370266601

Gene: CYP24A1

Linked Data

• dbSNP Id: rs2092654773
• gnomAD v4: 20-54162452-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.54162452A>G , CM000682.2:g.54162452A>G	GRCh38
NC_000020.10:g.52778991A>G , CM000682.1:g.52778991A>G	GRCh37
NC_000020.9:g.52212398A>G	NCBI36
NG_008334.1:g.16526T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000216862.8:c.990+265T>C MANE Select	ENSP00000216862.3:n.990+265T>C
ENST00000216862.7:c.990+265T>C	ENSP00000216862.3:n.990+265T>C
ENST00000395954.3:c.564+265T>C	ENSP00000379284.3:n.564+265T>C
ENST00000395955.7:c.990+265T>C	ENSP00000379285.3:n.990+265T>C
NM_000782.4:c.990+265T>C	NP_000773.2:n.990+265T>C
NM_001128915.1:c.990+265T>C	NP_001122387.1:n.990+265T>C
XM_005260304.3:c.990+265T>C	XP_005260361.1:n.990+265T>C
XM_005260304.5:c.990+265T>C	XP_005260361.1:n.990+265T>C
XM_017027691.2:c.990+265T>C	XP_016883180.1:n.990+265T>C
XM_017027692.2:c.990+265T>C	XP_016883181.1:n.990+265T>C
XM_017027693.2:c.990+265T>C	XP_016883182.1:n.990+265T>C
NM_000782.5:c.990+265T>C MANE Select	NP_000773.2:n.990+265T>C
NM_001128915.2:c.990+265T>C	NP_001122387.1:n.990+265T>C