Linked Data
gnomAD v4:
7-73683017-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.73683017C>A , CM000669.2:g.73683017C>A | GRCh38 |
| NC_000007.13:g.73097347C>A , CM000669.1:g.73097347C>A | GRCh37 |
| NC_000007.12:g.72735283C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000395176.3:c.407G>T MANE Select | ENSP00000378605.1:p.Gly136Val | |
| ENST00000395176.2:c.407G>T | ENSP00000378605.1:p.Gly136Val | |
| NM_032317.2:c.407G>T | NP_115693.2:p.Gly136Val | |
| NM_032317.3:c.407G>T MANE Select | NP_115693.2:p.Gly136Val |