Linked Data
dbSNP Id:
rs1362093037
gnomAD v2:
17-59668128-T-G
gnomAD v3:
17-61590767-T-G
gnomAD v4:
17-61590767-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.61590767T>G , CM000679.2:g.61590767T>G | GRCh38 |
| NC_000017.10:g.59668128T>G , CM000679.1:g.59668128T>G | GRCh37 |
| NC_000017.9:g.57022910T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000521764.3:c.414A>C MANE Select | ENSP00000427802.1:p.Ala138= | |
| ENST00000521764.2:c.414A>C | ENSP00000427802.1:p.Ala138= | |
| NM_199290.3:c.414A>C | NP_954984.1:p.Ala138= | |
| NM_199290.4:c.414A>C MANE Select | NP_954984.1:p.Ala138= |