HGVS | Genome Assembly |
---|---|
NC_000019.10:g.2274757G= , CM000681.2:g.2274757G= | GRCh38 |
NC_000019.9:g.2274756G= , CM000681.1:g.2274756G= | GRCh37 |
NC_000019.8:g.2225756G= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000342063.5:c.*923C= MANE Select | ENSP00000345102.3:n.*923C= | |
ENST00000342063.4:c.*923C= | ENSP00000345102.3:n.*923C= | |
ENST00000621615.1:c.146+5013G= | ENSP00000481965.1:n.146+5013G= | |
NM_198532.2:c.*923C= | NP_940934.1:n.*923C= | |
NM_198532.3:c.*923C= MANE Select | NP_940934.1:n.*923C= |