Linked Data
dbSNP Id:
rs1599602695
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.12887138C>T , CM000681.2:g.12887138C>T | GRCh38 |
| NC_000019.9:g.12997952C>T , CM000681.1:g.12997952C>T | GRCh37 |
| NC_000019.8:g.12858952C>T | NCBI36 |
| NG_009292.1:g.979C>T | |
| NG_013087.1:g.5066G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264834.6:c.3G>A MANE Select | ENSP00000264834.3:p.Met1Ile | |
| ENST00000264834.4:c.3G>A | ENSP00000264834.3:p.Met1Ile | |
| NM_006563.3:c.3G>A | NP_006554.1:p.Met1Ile | |
| NM_006563.4:c.3G>A | NP_006554.1:p.Met1Ile | |
| NM_006563.5:c.3G>A MANE Select | NP_006554.1:p.Met1Ile |