Linked Data
MyVariant Identifiers:
chr16:g.30748693A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.30737372A>T , CM000678.2:g.30737372A>T | GRCh38 |
| NC_000016.9:g.30748693A>T , CM000678.1:g.30748693A>T | GRCh37 |
| NC_000016.8:g.30656194A>T | NCBI36 |
| NG_032135.1:g.43232A>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000411466.7:c.7332A>T | ENSP00000405186.3:p.Arg2444= | |
| ENST00000704023.1:c.1593+19A>T | ||
| ENST00000706321.1:c.7332A>T | ENSP00000516346.1:p.Arg2444= | |
| ENST00000262518.9:c.7332A>T MANE Select | ENSP00000262518.4:p.Arg2444= | |
| ENST00000262518.8:c.7332A>T | ENSP00000262518.4:p.Arg2444= | |
| ENST00000380361.7:c.6801A>T | ENSP00000369719.3:p.Arg2267= | |
| ENST00000395059.6:c.6555A>T | ENSP00000378499.3:p.Arg2185= | |
| NM_006662.2:c.7332A>T | NP_006653.2:p.Arg2444= | |
| NM_006662.3:c.7332A>T MANE Select | NP_006653.2:p.Arg2444= |