Linked Data
dbSNP Id:
rs1723850360
gnomAD v4:
4-46993355-G-A
MyVariant Identifiers:
chr4:g.46995372G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.46993355G>A , CM000666.2:g.46993355G>A | GRCh38 |
| NC_000004.11:g.46995372G>A , CM000666.1:g.46995372G>A | GRCh37 |
| NC_000004.10:g.46690129G>A | NCBI36 |
| NG_011809.1:g.5209C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264318.4:c.70C>T MANE Select | ENSP00000264318.3:p.Leu24= | |
| ENST00000264318.3:c.70C>T | ENSP00000264318.3:p.Leu24= | |
| ENST00000502874.1:c.70C>T | ENSP00000424386.1:p.Leu24= | |
| ENST00000508560.5:c.18+52C>T | ENSP00000425445.1:n.18+52C>T | |
| ENST00000509316.1:n.194C>T | ||
| ENST00000511523.5:c.18+52C>T | ENSP00000422152.1:n.18+52C>T | |
| NM_000809.3:c.70C>T | NP_000800.2:p.Leu24= | |
| NM_001204266.1:c.29+52C>T | NP_001191195.1:n.29+52C>T | |
| NM_001204267.1:c.29+52C>T | NP_001191196.1:n.29+52C>T | |
| XM_011513677.1:c.70C>T | XP_011511979.1:p.Leu24= | |
| NM_000809.4:c.70C>T MANE Select | NP_000800.2:p.Leu24= | |
| NM_001204266.2:c.29+52C>T | NP_001191195.1:n.29+52C>T | |
| NM_001204267.2:c.29+52C>T | NP_001191196.1:n.29+52C>T |