Canonical Allele Identifier: CA400879960
Gene: COG1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.71189429T>G (hg19) chr17:g.73193290T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.73193290T>G , CM000679.2:g.73193290T>G GRCh38
NC_000017.10:g.71189429T>G , CM000679.1:g.71189429T>G GRCh37
NC_000017.9:g.68701024T>G NCBI36
NG_008971.1:g.5257T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000299886.9:c.221T>G MANE Select ENSP00000299886.4:p.Val74Gly
ENST00000299886.8:c.221T>G ENSP00000299886.4:p.Val74Gly
ENST00000438720.7:c.219T>G
ENST00000582587.2:c.198T>G
ENST00000618996.4:c.221T>G ENSP00000479450.1:p.Val74Gly
NM_018714.2:c.221T>G NP_061184.1:p.Val74Gly
NM_018714.3:c.221T>G MANE Select NP_061184.1:p.Val74Gly
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Search 100 bp 3'