Canonical Allele Identifier: CA875174595
Gene: OTC HGNC NCBI

Linked Data

dbSNP Id: rs1400280481
gnomAD v4: X-38403820-C-G
MyVariant Identifiers: chrX:g.38263073C>G (hg19) chrX:g.38403820C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38403820C>G , CM000685.2:g.38403820C>G GRCh38
NC_000023.10:g.38263073C>G , CM000685.1:g.38263073C>G GRCh37
NC_000023.9:g.38148017C>G NCBI36
NG_008471.1:g.56338C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000039007.5:c.663+80C>G MANE Select ENSP00000039007.4:n.663+80C>G
ENST00000643344.1:c.*413+80C>G ENSP00000496606.1:n.*413+80C>G
ENST00000039007.4:c.663+80C>G ENSP00000039007.4:n.663+80C>G
ENST00000465127.1:c.172-262301C>G ENSP00000417050.1:n.172-262301C>G
NM_000531.5:c.663+80C>G NP_000522.3:n.663+80C>G
XM_017029556.1:c.663+80C>G XP_016885045.1:n.663+80C>G
NM_000531.6:c.663+80C>G MANE Select NP_000522.3:n.663+80C>G
Search 100 bp 5'
Search 100 bp 3'