Canonical Allele Identifier: CA1018572451
Gene: CYP24A1 HGNC NCBI

Linked Data

dbSNP Id: rs2092703571

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.54173660G>A , CM000682.2:g.54173660G>A GRCh38
NC_000020.10:g.52790199G>A , CM000682.1:g.52790199G>A GRCh37
NC_000020.9:g.52223606G>A NCBI36
NG_008334.1:g.5318C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000216862.8:c.-81C>T MANE Select ENSP00000216862.3:n.-81C>T
ENST00000216862.7:c.-81C>T ENSP00000216862.3:n.-81C>T
NM_000782.4:c.-81C>T NP_000773.2:n.-81C>T
NM_001128915.1:c.-81C>T NP_001122387.1:n.-81C>T
XM_005260304.3:c.-81C>T XP_005260361.1:n.-81C>T
XM_005260304.5:c.-81C>T XP_005260361.1:n.-81C>T
XM_017027691.2:c.-81C>T XP_016883180.1:n.-81C>T
XM_017027692.2:c.-81C>T XP_016883181.1:n.-81C>T
XM_017027693.2:c.-81C>T XP_016883182.1:n.-81C>T
NM_000782.5:c.-81C>T MANE Select NP_000773.2:n.-81C>T
NM_001128915.2:c.-81C>T NP_001122387.1:n.-81C>T