Linked Data
gnomAD v4:
6-31861228-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31861228C>T , CM000668.2:g.31861228C>T | GRCh38 |
| NC_000006.11:g.31829005C>T , CM000668.1:g.31829005C>T | GRCh37 |
| NC_000006.10:g.31936984C>T | NCBI36 |
| NG_008201.1:g.6705G>A | |
| NG_023058.1:g.22819G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375631.5:c.575G>A MANE Select | ENSP00000364782.4:p.Gly192Asp | |
| ENST00000677054.1:n.1252G>A | ||
| ENST00000677512.1:n.683G>A | ||
| ENST00000678869.1:n.683G>A | ||
| ENST00000375631.4:c.575G>A | ENSP00000364782.4:p.Gly192Asp | |
| ENST00000480384.1:n.604G>A | ||
| ENST00000491768.5:c.575G>A | ENSP00000433127.1:p.Gly192Asp | |
| ENST00000495807.1:n.1143G>A | ||
| NM_000434.3:c.575G>A | NP_000425.1:p.Gly192Asp | |
| NM_000434.4:c.575G>A MANE Select | NP_000425.1:p.Gly192Asp |