HGVS | Genome Assembly |
---|---|
NC_000004.12:g.122613717A= , CM000666.2:g.122613717A= | GRCh38 |
NC_000004.11:g.123534872A= , CM000666.1:g.123534872A= | GRCh37 |
NC_000004.10:g.123754322A= | NCBI36 |
NG_031966.1:g.12341T= | |
NG_031966.2:g.12350T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000611104.2:c.361-789T= | ENSP00000477555.1:n.361-789T= | |
ENST00000647784.1:n.213-789T= | ||
ENST00000648588.1:c.361-789T= MANE Select | ENSP00000497915.1:n.361-789T= | |
ENST00000264497.7:c.361-789T= | ENSP00000264497.3:n.361-789T= | |
ENST00000611104.1:c.361-789T= | ENSP00000477555.1:n.361-789T= | |
NM_001207006.2:c.361-789T= | NP_001193935.1:n.361-789T= | |
NM_021803.3:c.361-789T= | NP_068575.1:n.361-789T= | |
NM_021803.4:c.361-789T= MANE Select | NP_068575.1:n.361-789T= | |
NM_001207006.3:c.361-789T= | NP_001193935.1:n.361-789T= |