Linked Data
ClinVar Variation Id:
594926
dbSNP Id:
rs1314994550
gnomAD v3:
10-89247607-G-A
gnomAD v4:
10-89247607-G-A
MyVariant Identifiers:
chr10:g.91007364G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.89247607G>A , CM000672.2:g.89247607G>A | GRCh38 |
| NC_000010.10:g.91007364G>A , CM000672.1:g.91007364G>A | GRCh37 |
| NC_000010.9:g.90997344G>A | NCBI36 |
| NG_008194.1:g.9297C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000336233.10:c.42C>T MANE Select | ENSP00000337354.5:p.Leu14= | |
| ENST00000282673.5:c.42C>T | ENSP00000282673.4:p.Leu14= | |
| ENST00000336233.9:c.42C>T | ENSP00000337354.5:p.Leu14= | |
| ENST00000371837.5:c.62-19209C>T | ENSP00000360903.1:n.62-19209C>T | |
| ENST00000428800.5:c.42C>T | ENSP00000388415.1:p.Leu14= | |
| ENST00000456827.5:c.-120+4130C>T | ENSP00000413019.2:n.-120+4130C>T | |
| NM_000235.3:c.42C>T | NP_000226.2:p.Leu14= | |
| NM_001127605.2:c.42C>T | NP_001121077.1:p.Leu14= | |
| NM_001288979.1:c.-120+4130C>T | NP_001275908.1:n.-120+4130C>T | |
| XM_024448023.1:c.42C>T | XP_024303791.1:p.Leu14= | |
| NM_000235.4:c.42C>T MANE Select | NP_000226.2:p.Leu14= | |
| NM_001127605.3:c.42C>T | NP_001121077.1:p.Leu14= | |
| NM_001288979.2:c.-120+4130C>T | NP_001275908.1:n.-120+4130C>T |