Linked Data
dbSNP Id:
rs1394508840
gnomAD v4:
8-117837191-G-T
MyVariant Identifiers:
chr8:g.118849430G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.117837191G>T , CM000670.2:g.117837191G>T | GRCh38 |
| NC_000008.10:g.118849430G>T , CM000670.1:g.118849430G>T | GRCh37 |
| NC_000008.9:g.118918611G>T | NCBI36 |
| NG_007455.2:g.279629C>A , LRG_493:g.279629C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684189.1:n.440C>A | ||
| ENST00000378204.7:c.973C>A MANE Select | ENSP00000367446.3:p.Arg325= | |
| ENST00000436216.2:c.341C>A | ||
| ENST00000378204.6:c.973C>A | ENSP00000367446.2:p.Arg325= | |
| ENST00000436216.1:c.341C>A | ||
| ENST00000437196.1:c.74-1640C>A | ENSP00000407299.1:n.74-1640C>A | |
| NM_000127.2:c.973C>A , LRG_493t1:c.973C>A | NP_000118.2:p.Arg325= | |
| NM_000127.3:c.973C>A MANE Select | NP_000118.2:p.Arg325= |