Canonical Allele Identifier: CA2653392400
Gene: CYP24A1 HGNC NCBI

Linked Data

dbSNP Id: rs2146517231

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.54173672C>G , CM000682.2:g.54173672C>G GRCh38
NC_000020.10:g.52790211C>G , CM000682.1:g.52790211C>G GRCh37
NC_000020.9:g.52223618C>G NCBI36
NG_008334.1:g.5306G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000216862.8:c.-93G>C MANE Select ENSP00000216862.3:n.-93G>C
ENST00000216862.7:c.-93G>C ENSP00000216862.3:n.-93G>C
NM_000782.4:c.-93G>C NP_000773.2:n.-93G>C
NM_001128915.1:c.-93G>C NP_001122387.1:n.-93G>C
XM_005260304.3:c.-93G>C XP_005260361.1:n.-93G>C
XM_005260304.5:c.-93G>C XP_005260361.1:n.-93G>C
XM_017027691.2:c.-93G>C XP_016883180.1:n.-93G>C
XM_017027692.2:c.-93G>C XP_016883181.1:n.-93G>C
XM_017027693.2:c.-93G>C XP_016883182.1:n.-93G>C
NM_000782.5:c.-93G>C MANE Select NP_000773.2:n.-93G>C
NM_001128915.2:c.-93G>C NP_001122387.1:n.-93G>C