Canonical Allele Identifier: CA363365416
Gene: LY6G6C HGNC NCBI
MPIG6B HGNC NCBI

Linked Data

dbSNP Id: rs1490092726
gnomAD v2: 6-31687021-T-C
gnomAD v3: 6-31719244-T-C
gnomAD v4: 6-31719244-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31719244T>C , CM000668.2:g.31719244T>C GRCh38
NC_000006.11:g.31687021T>C , CM000668.1:g.31687021T>C GRCh37
NC_000006.10:g.31795000T>C NCBI36
NG_029044.1:g.901T>C
NG_029044.2:g.901T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000375819.3:c.230A>G (LY6G6C) MANE Select ENSP00000364978.2:p.Asn77Ser
ENST00000375819.2:c.230A>G (LY6G6C) ENSP00000364978.2:p.Asn77Ser
ENST00000460663.5:n.90+561T>C (MPIG6B)
ENST00000495859.1:c.62A>G (LY6G6C) ENSP00000433207.1:p.Asn21Ser
NM_025261.2:c.230A>G (LY6G6C) NP_079537.1:p.Asn77Ser
NM_025261.3:c.230A>G (LY6G6C) MANE Select NP_079537.1:p.Asn77Ser