Linked Data
dbSNP Id:
rs2079243914
gnomAD v4:
16-31185027-C-T
MyVariant Identifiers:
chr16:g.31196348C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.31185027C>T , CM000678.2:g.31185027C>T | GRCh38 |
| NC_000016.9:g.31196348C>T , CM000678.1:g.31196348C>T | GRCh37 |
| NC_000016.8:g.31103849C>T | NCBI36 |
| NG_012889.2:g.9896C>T , LRG_655:g.9896C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000254108.12:c.612C>T MANE Select | ENSP00000254108.8:p.Gly204= | |
| ENST00000254108.11:c.612C>T | ENSP00000254108.7:p.Gly204= | |
| ENST00000380244.7:c.609C>T | ENSP00000369594.3:p.Gly203= | |
| ENST00000487509.6:n.677C>T | ||
| ENST00000566605.5:c.612C>T | ENSP00000455073.1:p.Gly204= | |
| ENST00000568685.1:c.612C>T | ENSP00000455282.1:p.Gly204= | |
| NM_001170634.1:c.609C>T | NP_001164105.1:p.Gly203= | |
| NM_001170937.1:c.600C>T | NP_001164408.1:p.Gly200= | |
| NM_004960.3:c.612C>T , LRG_655t1:c.612C>T | NP_004951.1:p.Gly204= | |
| NR_028388.2:n.717C>T | ||
| XM_005255233.3:c.32C>T | XP_005255290.1:p.Ala11Val | |
| XM_011545781.1:c.606C>T | XP_011544083.1:p.Gly202= | |
| XM_011545782.1:c.32C>T | XP_011544084.1:p.Ala11Val | |
| XM_005255233.5:c.32C>T | XP_005255290.1:p.Ala11Val | |
| XM_011545782.2:c.32C>T | XP_011544084.1:p.Ala11Val | |
| XM_024450221.1:c.603C>T | XP_024305989.1:p.Gly201= | |
| NM_004960.4:c.612C>T MANE Select | NP_004951.1:p.Gly204= |