Canonical Allele Identifier: CA385604288
Gene: GNS HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.65122782T>C (hg19) chr12:g.64729002T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.64729002T>C , CM000674.2:g.64729002T>C GRCh38
NC_000012.11:g.65122782T>C , CM000674.1:g.65122782T>C GRCh37
NC_000012.10:g.63409049T>C NCBI36
NG_008955.1:g.35445A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000258145.8:c.1154A>G MANE Select ENSP00000258145.3:p.Asp385Gly
ENST00000258145.7:c.1154A>G ENSP00000258145.3:p.Asp385Gly
ENST00000418919.6:c.986A>G ENSP00000413130.2:p.Asp329Gly
ENST00000537823.1:n.153A>G
ENST00000540196.5:c.557-5889A>G
ENST00000540883.1:n.217A>G
ENST00000541781.5:n.1209A>G
ENST00000542058.5:c.1094A>G ENSP00000444819.1:p.Asp365Gly
ENST00000543646.5:c.1250A>G ENSP00000438497.1:p.Asp417Gly
NM_002076.3:c.1154A>G NP_002067.1:p.Asp385Gly
NM_002076.4:c.1154A>G MANE Select NP_002067.1:p.Asp385Gly
Search 100 bp 5'
Search 100 bp 3'