Canonical Allele Identifier: CA2639622902
Gene: COG1 HGNC NCBI

Linked Data

gnomAD v4: 17-73196370-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.73196370A>T , CM000679.2:g.73196370A>T GRCh38
NC_000017.10:g.71192509A>T , CM000679.1:g.71192509A>T GRCh37
NC_000017.9:g.68704104A>T NCBI36
NG_008971.1:g.8337A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000299886.9:c.316-137A>T MANE Select ENSP00000299886.4:n.316-137A>T
ENST00000299886.8:c.316-137A>T ENSP00000299886.4:n.316-137A>T
ENST00000438720.7:c.314-137A>T
ENST00000582587.2:c.293-117A>T
ENST00000618996.4:c.316-137A>T ENSP00000479450.1:n.316-137A>T
NM_018714.2:c.316-137A>T NP_061184.1:n.316-137A>T
NM_018714.3:c.316-137A>T MANE Select NP_061184.1:n.316-137A>T
Search 100 bp 5'
Search 100 bp 3'