Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.93101702C>T , CM000669.2:g.93101702C>T | GRCh38 |
| NC_000007.13:g.92731015C>T , CM000669.1:g.92731015C>T | GRCh37 |
| NC_000007.12:g.92568951C>T | NCBI36 |
| NG_023419.1:g.21322G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_017654.4:c.4396G>A MANE Select | NP_060124.2:p.Gly1466Arg |
| ENST00000379958.3:c.4396G>A MANE Select | ENSP00000369292.2:p.Gly1466Arg |
| NM_001193307.1:c.4396G>A | NP_001180236.1:p.Gly1466Arg |
| NM_001193307.2:c.4396G>A | NP_001180236.1:p.Gly1466Arg |
| NM_017654.3:c.4396G>A | NP_060124.2:p.Gly1466Arg |
| ENST00000379958.2:c.4396G>A | ENSP00000369292.2:p.Gly1466Arg |
| ENST00000620985.4:c.4396G>A | ENSP00000484636.1:p.Gly1466Arg |