Canonical Allele Identifier: CA3720110
Gene: LY6G6C HGNC NCBI
MPIG6B HGNC NCBI

Linked Data

dbSNP Id: rs763926992
gnomAD v2: 6-31686928-A-G
gnomAD v4: 6-31719151-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31719151A>G , CM000668.2:g.31719151A>G GRCh38
NC_000006.11:g.31686928A>G , CM000668.1:g.31686928A>G GRCh37
NC_000006.10:g.31794907A>G NCBI36
NG_029044.1:g.808A>G
NG_029044.2:g.808A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375819.3:c.323T>C (LY6G6C) MANE Select ENSP00000364978.2:p.Leu108Pro
ENST00000375819.2:c.323T>C (LY6G6C) ENSP00000364978.2:p.Leu108Pro
ENST00000460663.5:n.90+468A>G (MPIG6B)
ENST00000495859.1:c.155T>C (LY6G6C) ENSP00000433207.1:p.Leu52Pro
NM_025261.2:c.323T>C (LY6G6C) NP_079537.1:p.Leu108Pro
NM_025261.3:c.323T>C (LY6G6C) MANE Select NP_079537.1:p.Leu108Pro