Canonical Allele Identifier: CA363365423
Gene: LY6G6C HGNC NCBI
MPIG6B HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31687022T>C (hg19) chr6:g.31719245T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31719245T>C , CM000668.2:g.31719245T>C GRCh38
NC_000006.11:g.31687022T>C , CM000668.1:g.31687022T>C GRCh37
NC_000006.10:g.31795001T>C NCBI36
NG_029044.1:g.902T>C
NG_029044.2:g.902T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000375819.3:c.229A>G (LY6G6C) MANE Select ENSP00000364978.2:p.Asn77Asp
ENST00000375819.2:c.229A>G (LY6G6C) ENSP00000364978.2:p.Asn77Asp
ENST00000460663.5:n.90+562T>C (MPIG6B)
ENST00000495859.1:c.61A>G (LY6G6C) ENSP00000433207.1:p.Asn21Asp
NM_025261.2:c.229A>G (LY6G6C) NP_079537.1:p.Asn77Asp
NM_025261.3:c.229A>G (LY6G6C) MANE Select NP_079537.1:p.Asn77Asp
Search 100 bp 5'
Search 100 bp 3'