Linked Data
dbSNP Id:
rs16951095
gnomAD v2:
18-7042911-C-T
gnomAD v3:
18-7042912-C-T
gnomAD v4:
18-7042912-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.7042912C>T , CM000680.2:g.7042912C>T | GRCh38 |
| NC_000018.9:g.7042911C>T , CM000680.1:g.7042911C>T | GRCh37 |
| NC_000018.8:g.7032911C>T | NCBI36 |
| NG_034251.1:g.79903G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000389658.4:c.1155+315G>A MANE Select | ENSP00000374309.3:n.1155+315G>A | |
| ENST00000389658.3:c.1155+315G>A | ENSP00000374309.3:n.1155+315G>A | |
| ENST00000579014.5:n.1509G>A | ||
| NM_005559.3:c.1155+315G>A | NP_005550.2:n.1155+315G>A | |
| XM_011525655.1:c.1155+315G>A | XP_011523957.1:n.1155+315G>A | |
| XM_011525657.1:c.1155+315G>A | XP_011523959.1:n.1155+315G>A | |
| XM_011525655.2:c.1155+315G>A | XP_011523957.1:n.1155+315G>A | |
| NM_005559.4:c.1155+315G>A MANE Select | NP_005550.2:n.1155+315G>A |