Canonical Allele Identifier: CA3720133
Gene: LY6G6C HGNC NCBI
MPIG6B HGNC NCBI

Linked Data

dbSNP Id: rs1488878633
gnomAD v2: 6-31687058-A-G
gnomAD v4: 6-31719281-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31719281A>G , CM000668.2:g.31719281A>G GRCh38
NC_000006.11:g.31687058A>G , CM000668.1:g.31687058A>G GRCh37
NC_000006.10:g.31795037A>G NCBI36
NG_029044.1:g.938A>G
NG_029044.2:g.938A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375819.3:c.193T>C (LY6G6C) MANE Select ENSP00000364978.2:p.Cys65Arg
ENST00000375819.2:c.193T>C (LY6G6C) ENSP00000364978.2:p.Cys65Arg
ENST00000460663.5:n.90+598A>G (MPIG6B)
ENST00000495859.1:c.25T>C (LY6G6C) ENSP00000433207.1:p.Cys9Arg
NM_025261.2:c.193T>C (LY6G6C) NP_079537.1:p.Cys65Arg
NM_025261.3:c.193T>C (LY6G6C) MANE Select NP_079537.1:p.Cys65Arg