Canonical Allele Identifier: CA363365292
Gene: LY6G6C HGNC NCBI
MPIG6B HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31686985G>A (hg19) chr6:g.31719208G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31719208G>A , CM000668.2:g.31719208G>A GRCh38
NC_000006.11:g.31686985G>A , CM000668.1:g.31686985G>A GRCh37
NC_000006.10:g.31794964G>A NCBI36
NG_029044.1:g.865G>A
NG_029044.2:g.865G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375819.3:c.266C>T (LY6G6C) MANE Select ENSP00000364978.2:p.Thr89Ile
ENST00000375819.2:c.266C>T (LY6G6C) ENSP00000364978.2:p.Thr89Ile
ENST00000460663.5:n.90+525G>A (MPIG6B)
ENST00000495859.1:c.98C>T (LY6G6C) ENSP00000433207.1:p.Thr33Ile
NM_025261.2:c.266C>T (LY6G6C) NP_079537.1:p.Thr89Ile
NM_025261.3:c.266C>T (LY6G6C) MANE Select NP_079537.1:p.Thr89Ile
Search 100 bp 5'
Search 100 bp 3'