Canonical Allele Identifier: CA363365014
Gene: LY6G6C HGNC NCBI
MPIG6B HGNC NCBI

Linked Data

dbSNP Id: rs1223027209
gnomAD v2: 6-31686919-A-G
gnomAD v4: 6-31719142-A-G
MyVariant Identifiers: chr6:g.31686919A>G (hg19) chr6:g.31719142A>G (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000375819.3:c.332T>C (LY6G6C) MANE Select ENSP00000364978.2:p.Val111Ala
ENST00000375819.2:c.332T>C (LY6G6C) ENSP00000364978.2:p.Val111Ala
ENST00000460663.5:n.90+459A>G (MPIG6B)
ENST00000495859.1:c.164T>C (LY6G6C) ENSP00000433207.1:p.Val55Ala
NM_025261.2:c.332T>C (LY6G6C) NP_079537.1:p.Val111Ala
NM_025261.3:c.332T>C (LY6G6C) MANE Select NP_079537.1:p.Val111Ala
Search 100 bp 5'
Search 100 bp 3'