MyVariant.info:
GRCh37
chr2:g.227661043T>A
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.226796327T>A , CM000664.2:g.226796327T>A | GRCh38 |
| NC_000002.11:g.227661043T>A , CM000664.1:g.227661043T>A | GRCh37 |
| NC_000002.10:g.227369287T>A | NCBI36 |
| NG_015830.1:g.7464A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000305123.6:c.2412A>T MANE Select | ENSP00000304895.4:p.Ala804= | |
| ENST00000305123.5:c.2412A>T | ENSP00000304895.4:p.Ala804= | |
| NM_005544.2:c.2412A>T | NP_005535.1:p.Ala804= | |
| NM_005544.3:c.2412A>T MANE Select | NP_005535.1:p.Ala804= |