HGVS | Genome Assembly |
---|---|
NC_000009.12:g.134408198C= , CM000671.2:g.134408198C= | GRCh38 |
NC_000009.11:g.137300044C= , CM000671.1:g.137300044C= | GRCh37 |
NC_000009.10:g.136439865C= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000481739.2:c.329C= MANE Select | ENSP00000419692.1:p.Pro110= | |
ENST00000672570.1:c.248C= | ENSP00000500402.1:p.Pro83= | |
ENST00000356384.4:n.739C= | ||
ENST00000481739.1:c.329C= | ENSP00000419692.1:p.Pro110= | |
NM_001291920.1:c.248C= | NP_001278849.1:p.Pro83= | |
NM_001291921.1:c.38C= | NP_001278850.1:p.Pro13= | |
NM_002957.5:c.329C= | NP_002948.1:p.Pro110= | |
NM_002957.6:c.329C= MANE Select | NP_002948.1:p.Pro110= | |
NM_001291921.2:c.38C= | NP_001278850.1:p.Pro13= | |
NM_001291920.2:c.248C= | NP_001278849.1:p.Pro83= |