Linked Data
dbSNP Id:
rs762044898
ExAC:
2:207632088 C / T
gnomAD v2:
2-207632088-C-T
gnomAD v4:
2-206767364-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.206767364C>T , CM000664.2:g.206767364C>T | GRCh38 |
| NC_000002.11:g.207632088C>T , CM000664.1:g.207632088C>T | GRCh37 |
| NC_000002.10:g.207340333C>T | NCBI36 |
| NG_008984.1:g.6977C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000402774.8:c.671C>T MANE Select | ENSP00000385990.3:p.Ala224Val | |
| ENST00000236980.10:c.671C>T | ENSP00000236980.6:p.Ala224Val | |
| ENST00000402774.7:c.671C>T | ENSP00000385990.3:p.Ala224Val | |
| ENST00000403094.3:c.671C>T | ENSP00000384929.3:p.Ala224Val | |
| ENST00000487777.5:n.729C>T | ||
| NM_001136193.1:c.671C>T | NP_001129665.1:p.Ala224Val | |
| NM_001136194.1:c.671C>T | NP_001129666.1:p.Ala224Val | |
| NM_014929.3:c.671C>T | NP_055744.2:p.Ala224Val | |
| NM_001136193.2:c.671C>T MANE Select | NP_001129665.1:p.Ala224Val | |
| NM_001136194.2:c.671C>T | NP_001129666.1:p.Ala224Val | |
| NM_014929.4:c.671C>T | NP_055744.2:p.Ala224Val |