HGVS | Genome Assembly |
---|---|
NC_000004.12:g.88008182_88008183insCG , CM000666.2:g.88008182_88008183insCG | GRCh38 |
NC_000004.11:g.88929334_88929335insCG , CM000666.1:g.88929334_88929335insCG | GRCh37 |
NC_000004.10:g.89148358_89148359insCG | NCBI36 |
NG_008604.1:g.5515_5516insCG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000237596.7:c.449_450insCG MANE Select | ENSP00000237596.2:p.Ser151GlyfsTer? | |
ENST00000237596.6:c.449_450insCG | ENSP00000237596.2:p.Ser151GlyfsTer? | |
NM_000297.3:c.449_450insCG | NP_000288.1:p.Ser151GlyfsTer? | |
XM_011532028.1:c.449_450insCG | XP_011530330.1:p.Ser151GlyfsTer? | |
XR_244632.2:n.544_545insCG | ||
NR_156488.1:n.536_537insCG | ||
XM_011532028.2:c.449_450insCG | XP_011530330.1:p.Ser151GlyfsTer? | |
NM_000297.4:c.449_450insCG MANE Select | NP_000288.1:p.Ser151GlyfsTer? | |
NR_156488.2:n.548_549insCG |