Canonical Allele Identifier: CA8739954
Gene: COG1 HGNC NCBI

Linked Data

dbSNP Id: rs147429178
ExAC: 17:71192723 C / A
gnomAD v2: 17-71192723-C-A
gnomAD v3: 17-73196584-C-A
gnomAD v4: 17-73196584-C-A
MyVariant Identifiers: chr17:g.71192723C>A (hg19) chr17:g.73196584C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.73196584C>A , CM000679.2:g.73196584C>A GRCh38
NC_000017.10:g.71192723C>A , CM000679.1:g.71192723C>A GRCh37
NC_000017.9:g.68704318C>A NCBI36
NG_008971.1:g.8551C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000299886.9:c.393C>A MANE Select ENSP00000299886.4:p.Ile131=
ENST00000299886.8:c.393C>A ENSP00000299886.4:p.Ile131=
ENST00000438720.7:c.391C>A
ENST00000582587.2:c.390C>A
ENST00000618996.4:c.393C>A ENSP00000479450.1:p.Ile131=
NM_018714.2:c.393C>A NP_061184.1:p.Ile131=
NM_018714.3:c.393C>A MANE Select NP_061184.1:p.Ile131=
Search 100 bp 5'
Search 100 bp 3'