Linked Data
dbSNP Id:
rs1423640595
gnomAD v2:
13-47409182-G-T
gnomAD v3:
13-46835047-G-T
gnomAD v4:
13-46835047-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.46835047G>T , CM000675.2:g.46835047G>T | GRCh38 |
| NC_000013.10:g.47409182G>T , CM000675.1:g.47409182G>T | GRCh37 |
| NC_000013.9:g.46307183G>T | NCBI36 |
| NG_013011.1:g.66988C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000542664.4:c.1206C>A MANE Select | ENSP00000437737.1:p.Asn402Lys | |
| ENST00000543956.5:c.717C>A | ENSP00000441861.2:p.Asn239Lys | |
| ENST00000378688.8:c.1206C>A | ENSP00000367959.3:p.Asn402Lys | |
| ENST00000542664.3:c.1206C>A | ENSP00000437737.1:p.Asn402Lys | |
| ENST00000543956.4:c.954C>A | ENSP00000441861.1:p.Asn318Lys | |
| NM_000621.4:c.1206C>A | NP_000612.1:p.Asn402Lys | |
| NM_001165947.2:c.954C>A | NP_001159419.1:p.Asn318Lys | |
| NM_000621.5:c.1206C>A MANE Select | NP_000612.1:p.Asn402Lys | |
| NM_001165947.5:c.717C>A | NP_001159419.2:p.Asn239Lys | |
| NM_001378924.1:c.1206C>A | NP_001365853.1:p.Asn402Lys |