Linked Data
dbSNP Id:
rs1224038883
gnomAD v3:
14-91272910-G-C
gnomAD v4:
14-91272910-G-C
MyVariant Identifiers:
chr14:g.91739254G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.91272910G>C , CM000676.2:g.91272910G>C | GRCh38 |
| NC_000014.8:g.91739254G>C , CM000676.1:g.91739254G>C | GRCh37 |
| NC_000014.7:g.90809007G>C | NCBI36 |
| NG_033118.1:g.149935C>G | |
| NG_033118.2:g.149935C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000389857.11:c.5802C>G MANE Select | ENSP00000374507.6:p.Ala1934= | |
| ENST00000331194.8:c.1236C>G | ENSP00000330332.8:p.Ala412= | |
| ENST00000389857.10:c.5802C>G | ENSP00000374507.6:p.Ala1934= | |
| ENST00000556726.5:c.2030C>G | ||
| NM_001080414.3:c.5802C>G | NP_001073883.2:p.Ala1934= | |
| XM_011536796.1:c.5694C>G | XP_011535098.1:p.Ala1898= | |
| XM_011536796.2:c.5694C>G | XP_011535098.1:p.Ala1898= | |
| XM_017021336.1:c.2883C>G | XP_016876825.1:p.Ala961= | |
| NM_001080414.4:c.5802C>G MANE Select | NP_001073883.2:p.Ala1934= |