Canonical Allele Identifier: CA363365013
Gene: LY6G6C HGNC NCBI
MPIG6B HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31686919A>C (hg19) chr6:g.31719142A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31719142A>C , CM000668.2:g.31719142A>C GRCh38
NC_000006.11:g.31686919A>C , CM000668.1:g.31686919A>C GRCh37
NC_000006.10:g.31794898A>C NCBI36
NG_029044.1:g.799A>C
NG_029044.2:g.799A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000375819.3:c.332T>G (LY6G6C) MANE Select ENSP00000364978.2:p.Val111Gly
ENST00000375819.2:c.332T>G (LY6G6C) ENSP00000364978.2:p.Val111Gly
ENST00000460663.5:n.90+459A>C (MPIG6B)
ENST00000495859.1:c.164T>G (LY6G6C) ENSP00000433207.1:p.Val55Gly
NM_025261.2:c.332T>G (LY6G6C) NP_079537.1:p.Val111Gly
NM_025261.3:c.332T>G (LY6G6C) MANE Select NP_079537.1:p.Val111Gly
Search 100 bp 5'
Search 100 bp 3'