Linked Data
ClinVar Variation Id:
2202455
ClinVar RCV Id:
RCV002664087
dbSNP Id:
rs1060504778
gnomAD v4:
19-4117443-G-C
MyVariant Identifiers:
chr19:g.4117441G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.4117443G>C , CM000681.2:g.4117443G>C | GRCh38 |
| NC_000019.9:g.4117441G>C , CM000681.1:g.4117441G>C | GRCh37 |
| NC_000019.8:g.4068441G>C | NCBI36 |
| NG_007996.1:g.11686C>G , LRG_750:g.11686C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000394867.9:n.718C>G | ||
| ENST00000687128.1:n.718C>G | ||
| ENST00000262948.10:c.279C>G MANE Select | ENSP00000262948.4:p.Pro93= | |
| ENST00000262948.9:c.279C>G | ENSP00000262948.3:p.Pro93= | |
| ENST00000394867.8:c.-13C>G | ENSP00000378336.1:n.-13C>G | |
| ENST00000599345.1:n.476C>G | ||
| NM_030662.3:c.279C>G , LRG_750t1:c.279C>G | NP_109587.1:p.Pro93= | |
| XM_006722799.2:c.279C>G | XP_006722862.1:p.Pro93= | |
| XM_017026989.1:c.279C>G | XP_016882478.1:p.Pro93= | |
| XM_017026990.1:c.279C>G | XP_016882479.1:p.Pro93= | |
| XM_017026991.1:c.279C>G | XP_016882480.1:p.Pro93= | |
| NM_030662.4:c.279C>G MANE Select | NP_109587.1:p.Pro93= |