HGVS | Genome Assembly |
---|---|
NC_000002.12:g.135817659C>G , CM000664.2:g.135817659C>G | GRCh38 |
NC_000002.11:g.136575229C>G , CM000664.1:g.136575229C>G | GRCh37 |
NC_000002.10:g.136291699C>G | NCBI36 |
NG_008104.2:g.42511G>C , LRG_338:g.42511G>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000264162.7:c.1389G>C MANE Select | ENSP00000264162.2:p.Met463Ile | |
ENST00000264162.6:c.1389G>C | ENSP00000264162.2:p.Met463Ile | |
NM_002299.2:c.1389G>C , LRG_338t1:c.1389G>C | NP_002290.2:p.Met463Ile | |
NM_002299.3:c.1389G>C | NP_002290.2:p.Met463Ile | |
XM_017004088.2:c.1389G>C | XP_016859577.1:p.Met463Ile | |
NM_002299.4:c.1389G>C MANE Select | NP_002290.2:p.Met463Ile |