Canonical Allele Identifier: CA1018572467
Gene: CYP24A1 HGNC NCBI

Linked Data

dbSNP Id: rs144737632
gnomAD v3: 20-54173679-A-T
gnomAD v4: 20-54173679-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.54173679A>T , CM000682.2:g.54173679A>T GRCh38
NC_000020.10:g.52790218A>T , CM000682.1:g.52790218A>T GRCh37
NC_000020.9:g.52223625A>T NCBI36
NG_008334.1:g.5299T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000216862.8:c.-100T>A MANE Select ENSP00000216862.3:n.-100T>A
ENST00000216862.7:c.-100T>A ENSP00000216862.3:n.-100T>A
NM_000782.4:c.-100T>A NP_000773.2:n.-100T>A
NM_001128915.1:c.-100T>A NP_001122387.1:n.-100T>A
XM_005260304.3:c.-100T>A XP_005260361.1:n.-100T>A
XM_005260304.5:c.-100T>A XP_005260361.1:n.-100T>A
XM_017027691.2:c.-100T>A XP_016883180.1:n.-100T>A
XM_017027692.2:c.-100T>A XP_016883181.1:n.-100T>A
XM_017027693.2:c.-100T>A XP_016883182.1:n.-100T>A
NM_000782.5:c.-100T>A MANE Select NP_000773.2:n.-100T>A
NM_001128915.2:c.-100T>A NP_001122387.1:n.-100T>A
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