Linked Data
ClinVar Variation Id:
1618566
ClinVar RCV Id:
RCV002093995
dbSNP Id:
rs573085618
ExAC:
14:55369237 G / C
gnomAD v2:
14-55369237-G-C
gnomAD v3:
14-54902519-G-C
gnomAD v4:
14-54902519-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.54902519G>C , CM000676.2:g.54902519G>C | GRCh38 |
| NC_000014.8:g.55369237G>C , CM000676.1:g.55369237G>C | GRCh37 |
| NC_000014.7:g.54438987G>C | NCBI36 |
| NG_008647.1:g.5306C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000491895.7:c.145C>G MANE Select | ENSP00000419045.2:p.Pro49Ala | |
| ENST00000254299.8:n.293C>G | ||
| ENST00000395514.5:c.145C>G | ENSP00000378890.1:p.Pro49Ala | |
| ENST00000491895.6:c.145C>G | ENSP00000419045.2:p.Pro49Ala | |
| ENST00000536224.2:c.145C>G | ENSP00000445246.2:p.Pro49Ala | |
| ENST00000543643.6:c.145C>G | ENSP00000444011.2:p.Pro49Ala | |
| ENST00000622544.4:c.145C>G | ENSP00000477796.1:p.Pro49Ala | |
| NM_000161.2:c.145C>G | NP_000152.1:p.Pro49Ala | |
| NM_001024024.1:c.145C>G | NP_001019195.1:p.Pro49Ala | |
| NM_001024070.1:c.145C>G | NP_001019241.1:p.Pro49Ala | |
| NM_001024071.1:c.145C>G | NP_001019242.1:p.Pro49Ala | |
| XM_005267530.1:c.145C>G | XP_005267587.1:p.Pro49Ala | |
| XM_011536643.1:c.145C>G | XP_011534945.1:p.Pro49Ala | |
| NM_000161.3:c.145C>G MANE Select | NP_000152.1:p.Pro49Ala | |
| NM_001024070.2:c.145C>G | NP_001019241.1:p.Pro49Ala | |
| NM_001024071.2:c.145C>G | NP_001019242.1:p.Pro49Ala | |
| NM_001024024.2:c.145C>G | NP_001019195.1:p.Pro49Ala |