Canonical Allele Identifier: CA449669421
Gene: LY6G6C HGNC NCBI
MPIG6B HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31686909G>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31719132G>C , CM000668.2:g.31719132G>C GRCh38
NC_000006.11:g.31686909G>C , CM000668.1:g.31686909G>C GRCh37
NC_000006.10:g.31794888G>C NCBI36
NG_029044.1:g.789G>C
NG_029044.2:g.789G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000375819.3:c.342C>G (LY6G6C) MANE Select ENSP00000364978.2:p.Thr114=
ENST00000375819.2:c.342C>G (LY6G6C) ENSP00000364978.2:p.Thr114=
ENST00000460663.5:n.90+449G>C (MPIG6B)
ENST00000495859.1:c.174C>G (LY6G6C) ENSP00000433207.1:p.Thr58=
NM_025261.2:c.342C>G (LY6G6C) NP_079537.1:p.Thr114=
NM_025261.3:c.342C>G (LY6G6C) MANE Select NP_079537.1:p.Thr114=
Search 100 bp 5'
Search 100 bp 3'