Canonical Allele Identifier: CA501714496
Gene: COG1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.71189517C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.73193378C>G , CM000679.2:g.73193378C>G GRCh38
NC_000017.10:g.71189517C>G , CM000679.1:g.71189517C>G GRCh37
NC_000017.9:g.68701112C>G NCBI36
NG_008971.1:g.5345C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000299886.9:c.309C>G MANE Select ENSP00000299886.4:p.Ala103=
ENST00000299886.8:c.309C>G ENSP00000299886.4:p.Ala103=
ENST00000438720.7:c.307C>G
ENST00000582587.2:c.286C>G
ENST00000618996.4:c.309C>G ENSP00000479450.1:p.Ala103=
NM_018714.2:c.309C>G NP_061184.1:p.Ala103=
NM_018714.3:c.309C>G MANE Select NP_061184.1:p.Ala103=