Canonical Allele Identifier: CA502026767
Gene: COG1 HGNC NCBI

Linked Data

dbSNP Id: rs1413662581
gnomAD v2: 17-71189433-G-A
gnomAD v3: 17-73193294-G-A
gnomAD v4: 17-73193294-G-A
MyVariant Identifiers: chr17:g.71189433G>A (hg19) chr17:g.73193294G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.73193294G>A , CM000679.2:g.73193294G>A GRCh38
NC_000017.10:g.71189433G>A , CM000679.1:g.71189433G>A GRCh37
NC_000017.9:g.68701028G>A NCBI36
NG_008971.1:g.5261G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000299886.9:c.225G>A MANE Select ENSP00000299886.4:p.Gly75=
ENST00000299886.8:c.225G>A ENSP00000299886.4:p.Gly75=
ENST00000438720.7:c.223G>A
ENST00000582587.2:c.202G>A
ENST00000618996.4:c.225G>A ENSP00000479450.1:p.Gly75=
NM_018714.2:c.225G>A NP_061184.1:p.Gly75=
NM_018714.3:c.225G>A MANE Select NP_061184.1:p.Gly75=
Search 100 bp 5'
Search 100 bp 3'