Canonical Allele Identifier: CA2086122664
Gene: COG6 HGNC NCBI

Linked Data

dbSNP Id: rs1881472520
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.39776655A>T , CM000675.2:g.39776655A>T GRCh38
NC_000013.10:g.40350792A>T , CM000675.1:g.40350792A>T GRCh37
NC_000013.9:g.39248792A>T NCBI36
NG_028352.1:g.126029A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000416691.5:c.1827-11680A>T ENSP00000403733.1:n.1827-11680A>T
NM_001145079.1:c.1827-11680A>T NP_001138551.1:n.1827-11680A>T
NM_001145079.2:c.1827-11680A>T NP_001138551.1:n.1827-11680A>T
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