HGVS | Genome Assembly |
---|---|
NC_000005.10:g.1416107T>G , CM000667.2:g.1416107T>G | GRCh38 |
NC_000005.9:g.1416222T>G , CM000667.1:g.1416222T>G | GRCh37 |
NC_000005.8:g.1469222T>G | NCBI36 |
NG_015885.1:g.34322A>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000270349.12:c.1022A>C MANE Select | ENSP00000270349.9:p.Asn341Thr | |
ENST00000270349.11:c.1022A>C | ENSP00000270349.9:p.Asn341Thr | |
ENST00000511750.1:n.472A>C | ||
NM_001044.4:c.1022A>C | NP_001035.1:p.Asn341Thr | |
NM_001044.5:c.1022A>C MANE Select | NP_001035.1:p.Asn341Thr |