Canonical Allele Identifier: CA3720108

Gene: LY6G6C MPIG6B

Linked Data

• dbSNP Id: rs752751364
• ExAC: 6:31686918 G / T
• gnomAD v2: 6-31686918-G-T
• gnomAD v4: 6-31719141-G-T
• MyVariant Identifiers: chr6:g.31686918G>T (hg19) ; chr6:g.31719141G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31719141G>T , CM000668.2:g.31719141G>T	GRCh38
NC_000006.11:g.31686918G>T , CM000668.1:g.31686918G>T	GRCh37
NC_000006.10:g.31794897G>T	NCBI36
NG_029044.1:g.798G>T
NG_029044.2:g.798G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375819.3:c.333C>A (LY6G6C) MANE Select	ENSP00000364978.2:p.Val111=
ENST00000375819.2:c.333C>A (LY6G6C)	ENSP00000364978.2:p.Val111=
ENST00000460663.5:n.90+458G>T (MPIG6B)
ENST00000495859.1:c.165C>A (LY6G6C)	ENSP00000433207.1:p.Val55=
NM_025261.2:c.333C>A (LY6G6C)	NP_079537.1:p.Val111=
NM_025261.3:c.333C>A (LY6G6C) MANE Select	NP_079537.1:p.Val111=