HGVS | Genome Assembly |
---|---|
NC_000010.11:g.99844383T>C , CM000672.2:g.99844383T>C | GRCh38 |
NC_000010.10:g.101604140T>C , CM000672.1:g.101604140T>C | GRCh37 |
NC_000010.9:g.101594130T>C | NCBI36 |
NG_011798.1:g.66678T>C | |
NG_011798.2:g.66786T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000647814.1:c.3905T>C MANE Select | ENSP00000497274.1:p.Phe1302Ser | |
ENST00000649459.1:n.253T>C | ||
ENST00000370449.8:c.3905T>C | ENSP00000359478.4:p.Phe1302Ser | |
NM_000392.4:c.3905T>C | NP_000383.1:p.Phe1302Ser | |
XM_006717630.2:c.3209T>C | XP_006717693.1:p.Phe1070Ser | |
XR_945604.1:n.4094T>C | ||
XR_945605.1:n.3969T>C | ||
NM_000392.5:c.3905T>C MANE Select | NP_000383.2:p.Phe1302Ser | |
XM_006717630.3:c.3209T>C | XP_006717693.1:p.Phe1070Ser | |
XR_945604.3:n.4148T>C | ||
XR_945605.3:n.4021T>C |