Canonical Allele Identifier: CA363365079
Gene: LY6G6C HGNC NCBI
MPIG6B HGNC NCBI

Linked Data

ClinVar Variation Id: 3121619
ClinVar RCV Id: RCV004410954
dbSNP Id: rs1806642170
MyVariant Identifiers: chr6:g.31686937G>T (hg19) chr6:g.31719160G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31719160G>T , CM000668.2:g.31719160G>T GRCh38
NC_000006.11:g.31686937G>T , CM000668.1:g.31686937G>T GRCh37
NC_000006.10:g.31794916G>T NCBI36
NG_029044.1:g.817G>T
NG_029044.2:g.817G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000375819.3:c.314C>A (LY6G6C) MANE Select ENSP00000364978.2:p.Thr105Asn
ENST00000375819.2:c.314C>A (LY6G6C) ENSP00000364978.2:p.Thr105Asn
ENST00000460663.5:n.90+477G>T (MPIG6B)
ENST00000495859.1:c.146C>A (LY6G6C) ENSP00000433207.1:p.Thr49Asn
NM_025261.2:c.314C>A (LY6G6C) NP_079537.1:p.Thr105Asn
NM_025261.3:c.314C>A (LY6G6C) MANE Select NP_079537.1:p.Thr105Asn
Search 100 bp 5'
Search 100 bp 3'