Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.6714213T>G , CM000681.2:g.6714213T>G | GRCh38 |
| NC_000019.9:g.6714224T>G , CM000681.1:g.6714224T>G | GRCh37 |
| NC_000019.8:g.6665224T>G | NCBI36 |
| NG_009557.1:g.11439A>C , LRG_27:g.11439A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695652.1:c.512A>C | ENSP00000512083.1:p.Asn171Thr | |
| ENST00000245907.11:c.635A>C MANE Select | ENSP00000245907.4:p.Asn212Thr | |
| ENST00000245907.10:c.635A>C | ENSP00000245907.4:p.Asn212Thr | |
| ENST00000595577.1:n.139A>C | ||
| NM_000064.3:c.635A>C | NP_000055.2:p.Asn212Thr | |
| NM_000064.4:c.635A>C MANE Select | NP_000055.2:p.Asn212Thr |