Canonical Allele Identifier: CA875144519
Gene: OTC HGNC NCBI

Linked Data

dbSNP Id: rs1186029769
gnomAD v4: X-38369731-T-A
MyVariant Identifiers: chrX:g.38228984T>A (hg19) chrX:g.38369731T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38369731T>A , CM000685.2:g.38369731T>A GRCh38
NC_000023.10:g.38228984T>A , CM000685.1:g.38228984T>A GRCh37
NC_000023.9:g.38113928T>A NCBI36
NG_008471.1:g.22249T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000039007.5:c.217-65T>A MANE Select ENSP00000039007.4:n.217-65T>A
ENST00000643344.1:c.217-65T>A ENSP00000496606.1:n.217-65T>A
ENST00000039007.4:c.217-65T>A ENSP00000039007.4:n.217-65T>A
ENST00000465127.1:c.172-296390T>A ENSP00000417050.1:n.172-296390T>A
ENST00000488812.1:n.309-65T>A
NM_000531.5:c.217-65T>A NP_000522.3:n.217-65T>A
XM_017029556.1:c.217-65T>A XP_016885045.1:n.217-65T>A
NM_000531.6:c.217-65T>A MANE Select NP_000522.3:n.217-65T>A
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