HGVS | Genome Assembly |
---|---|
NC_000002.12:g.240872990T>C , CM000664.2:g.240872990T>C | GRCh38 |
NC_000002.11:g.241812407T>C , CM000664.1:g.241812407T>C | GRCh37 |
NC_000002.10:g.241461080T>C | NCBI36 |
NG_008005.1:g.9246T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307503.4:c.536T>C MANE Select | ENSP00000302620.3:p.Leu179Pro | |
ENST00000307503.3:c.536T>C | ENSP00000302620.3:p.Leu179Pro | |
ENST00000472436.1:n.556T>C | ||
ENST00000476698.1:n.273T>C | ||
NM_000030.2:c.536T>C | NP_000021.1:p.Leu179Pro | |
NM_000030.3:c.536T>C MANE Select | NP_000021.1:p.Leu179Pro |