HGVS | Genome Assembly |
---|---|
NC_000002.12:g.73641075A>C , CM000664.2:g.73641075A>C | GRCh38 |
NC_000002.11:g.73868202A>C , CM000664.1:g.73868202A>C | GRCh37 |
NC_000002.10:g.73721710A>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000272425.4:c.554T>G MANE Select | ENSP00000272425.3:p.Met185Arg | |
ENST00000272425.3:c.554T>G | ENSP00000272425.3:p.Met185Arg | |
NM_003960.3:c.554T>G | NP_003951.3:p.Met185Arg | |
NM_003960.4:c.554T>G MANE Select | NP_003951.3:p.Met185Arg |