Canonical Allele Identifier: CA502026770
Gene: COG1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.71189436A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.73193297A>G , CM000679.2:g.73193297A>G GRCh38
NC_000017.10:g.71189436A>G , CM000679.1:g.71189436A>G GRCh37
NC_000017.9:g.68701031A>G NCBI36
NG_008971.1:g.5264A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000299886.9:c.228A>G MANE Select ENSP00000299886.4:p.Leu76=
ENST00000299886.8:c.228A>G ENSP00000299886.4:p.Leu76=
ENST00000438720.7:c.226A>G
ENST00000582587.2:c.205A>G
ENST00000618996.4:c.228A>G ENSP00000479450.1:p.Leu76=
NM_018714.2:c.228A>G NP_061184.1:p.Leu76=
NM_018714.3:c.228A>G MANE Select NP_061184.1:p.Leu76=