Canonical Allele Identifier: CA363364990

Gene: LY6G6C MPIG6B

Linked Data

• MyVariant Identifiers: chr6:g.31686913A>T (hg19) ; chr6:g.31719136A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31719136A>T , CM000668.2:g.31719136A>T	GRCh38
NC_000006.11:g.31686913A>T , CM000668.1:g.31686913A>T	GRCh37
NC_000006.10:g.31794892A>T	NCBI36
NG_029044.1:g.793A>T
NG_029044.2:g.793A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375819.3:c.338T>A (LY6G6C) MANE Select	ENSP00000364978.2:p.Leu113His
ENST00000375819.2:c.338T>A (LY6G6C)	ENSP00000364978.2:p.Leu113His
ENST00000460663.5:n.90+453A>T (MPIG6B)
ENST00000495859.1:c.170T>A (LY6G6C)	ENSP00000433207.1:p.Leu57His
NM_025261.2:c.338T>A (LY6G6C)	NP_079537.1:p.Leu113His
NM_025261.3:c.338T>A (LY6G6C) MANE Select	NP_079537.1:p.Leu113His