HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31719234G>T , CM000668.2:g.31719234G>T | GRCh38 |
NC_000006.11:g.31687011G>T , CM000668.1:g.31687011G>T | GRCh37 |
NC_000006.10:g.31794990G>T | NCBI36 |
NG_029044.1:g.891G>T | |
NG_029044.2:g.891G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375819.3:c.240C>A (LY6G6C) MANE Select | ENSP00000364978.2:p.Asn80Lys | |
ENST00000375819.2:c.240C>A (LY6G6C) | ENSP00000364978.2:p.Asn80Lys | |
ENST00000460663.5:n.90+551G>T (MPIG6B) | ||
ENST00000495859.1:c.72C>A (LY6G6C) | ENSP00000433207.1:p.Asn24Lys | |
NM_025261.2:c.240C>A (LY6G6C) | NP_079537.1:p.Asn80Lys | |
NM_025261.3:c.240C>A (LY6G6C) MANE Select | NP_079537.1:p.Asn80Lys |