Canonical Allele Identifier: CA2370272057
Gene: CYP24A1 HGNC NCBI

Linked Data

dbSNP Id: rs1601153016

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.54173743A>C , CM000682.2:g.54173743A>C GRCh38
NC_000020.10:g.52790282A>C , CM000682.1:g.52790282A>C GRCh37
NC_000020.9:g.52223689A>C NCBI36
NG_008334.1:g.5235T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000216862.8:c.-164T>G MANE Select ENSP00000216862.3:n.-164T>G
ENST00000216862.7:c.-164T>G ENSP00000216862.3:n.-164T>G
NM_000782.4:c.-164T>G NP_000773.2:n.-164T>G
NM_001128915.1:c.-164T>G NP_001122387.1:n.-164T>G
XM_005260304.3:c.-164T>G XP_005260361.1:n.-164T>G
XM_005260304.5:c.-164T>G XP_005260361.1:n.-164T>G
XM_017027691.2:c.-164T>G XP_016883180.1:n.-164T>G
XM_017027692.2:c.-164T>G XP_016883181.1:n.-164T>G
XM_017027693.2:c.-164T>G XP_016883182.1:n.-164T>G
NM_000782.5:c.-164T>G MANE Select NP_000773.2:n.-164T>G
NM_001128915.2:c.-164T>G NP_001122387.1:n.-164T>G