HGVS | Genome Assembly |
---|---|
NC_000011.10:g.119341600T>C , CM000673.2:g.119341600T>C | GRCh38 |
NC_000011.9:g.119212310T>C , CM000673.1:g.119212310T>C | GRCh37 |
NC_000011.8:g.118717520T>C | NCBI36 |
NG_012235.1:g.10074A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000619721.6:c.1688A>G (MFRP) MANE Select | ENSP00000481824.1:p.Asn563Ser | |
ENST00000360167.4:c.1334A>G (MFRP) | ENSP00000353291.4:p.Asn445Ser | |
ENST00000449574.7:c.559A>G (MFRP) | ||
ENST00000619721.5:c.1688A>G (MFRP) | ENSP00000481824.1:p.Asn563Ser | |
NM_015645.4:c.-949A>G (C1QTNF5) | NP_056460.1:n.-949A>G | |
NM_031433.3:c.1688A>G (MFRP) | NP_113621.1:p.Asn563Ser | |
NM_031433.4:c.1688A>G (MFRP) MANE Select | NP_113621.1:p.Asn563Ser | |
NM_015645.5:c.-949A>G (C1QTNF5) | NP_056460.1:n.-949A>G |