Canonical Allele Identifier: CA3720123
Gene: LY6G6C HGNC NCBI
MPIG6B HGNC NCBI

Linked Data

dbSNP Id: rs538733367
ExAC: 6:31687009 C / T
gnomAD v2: 6-31687009-C-T
gnomAD v3: 6-31719232-C-T
gnomAD v4: 6-31719232-C-T
COSMIC: COSM1643004
MyVariant Identifiers: chr6:g.31687009C>T (hg19) chr6:g.31719232C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31719232C>T , CM000668.2:g.31719232C>T GRCh38
NC_000006.11:g.31687009C>T , CM000668.1:g.31687009C>T GRCh37
NC_000006.10:g.31794988C>T NCBI36
NG_029044.1:g.889C>T
NG_029044.2:g.889C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000375819.3:c.242G>A (LY6G6C) MANE Select ENSP00000364978.2:p.Arg81His
ENST00000375819.2:c.242G>A (LY6G6C) ENSP00000364978.2:p.Arg81His
ENST00000460663.5:n.90+549C>T (MPIG6B)
ENST00000495859.1:c.74G>A (LY6G6C) ENSP00000433207.1:p.Arg25His
NM_025261.2:c.242G>A (LY6G6C) NP_079537.1:p.Arg81His
NM_025261.3:c.242G>A (LY6G6C) MANE Select NP_079537.1:p.Arg81His
Search 100 bp 5'
Search 100 bp 3'