Linked Data
ClinVar Variation Id:
794768
dbSNP Id:
rs1596223055
gnomAD v4:
16-2046248-G-C
MyVariant Identifiers:
chr16:g.2096249G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.2046248G>C , CM000678.2:g.2046248G>C | GRCh38 |
| NC_000016.9:g.2096249G>C , CM000678.1:g.2096249G>C | GRCh37 |
| NC_000016.8:g.2036250G>C | NCBI36 |
| NG_005895.1:g.1943G>C , LRG_487:g.1943G>C | |
| NG_008412.1:g.6619C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000651570.2:c.234C>G MANE Select | ENSP00000498421.1:p.Val78= | |
| ENST00000651583.1:c.189C>G | ENSP00000498821.1:p.Val63= | |
| ENST00000219066.5:c.258C>G | ENSP00000219066.1:p.Val86= | |
| ENST00000561841.1:c.154C>G | ||
| ENST00000566380.5:c.197C>G | ||
| ENST00000568513.5:c.173+32C>G | ||
| NM_002528.5:c.258C>G | NP_002519.1:p.Val86= | |
| XM_011522505.1:c.258C>G | XP_011520807.1:p.Val86= | |
| NM_001318193.1:c.258C>G | NP_001305122.1:p.Val86= | |
| NM_001318194.1:c.24+32C>G | NP_001305123.1:n.24+32C>G | |
| NM_002528.6:c.258C>G | NP_002519.1:p.Val86= | |
| XM_017023253.1:c.258C>G | XP_016878742.1:p.Val86= | |
| NM_001318193.2:c.234C>G | NP_001305122.2:p.Val78= | |
| NM_002528.7:c.234C>G MANE Select | NP_002519.2:p.Val78= | |
| NM_001318194.2:c.24+32C>G | NP_001305123.1:n.24+32C>G |