Linked Data
dbSNP Id:
rs201297021
gnomAD v4:
22-42127894-C-G
MyVariant Identifiers:
chr22:g.42523896C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.42127894C>G , CM000684.2:g.42127894C>G | GRCh38 |
| NC_000022.10:g.42523896C>G , CM000684.1:g.42523896C>G | GRCh37 |
| NC_000022.9:g.40853840C>G | NCBI36 |
| NG_008376.3:g.7098G>C | |
| NG_008376.4:g.7917G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360124.10:c.731G>C | ENSP00000353241.6:n.731G>C | |
| ENST00000645361.2:c.933G>C MANE Select | ENSP00000496150.1:p.Ser311= | |
| ENST00000359033.4:c.780G>C | ENSP00000351927.4:p.Ser260= | |
| ENST00000360124.9:c.551G>C | ENSP00000353241.5:n.551G>C | |
| ENST00000360608.9:c.933G>C | ENSP00000353820.5:p.Ser311= | |
| ENST00000389970.7:c.867G>C | ENSP00000374620.4:p.Ser289= | |
| ENST00000488442.1:n.1657G>C | ||
| NM_000106.5:c.933G>C | NP_000097.3:p.Ser311= | |
| NM_001025161.2:c.780G>C | NP_001020332.2:p.Ser260= | |
| XM_011529966.1:c.933G>C | XP_011528268.1:p.Ser311= | |
| XM_011529967.1:c.933G>C | XP_011528269.1:p.Ser311= | |
| XM_011529968.1:c.933G>C | XP_011528270.1:p.Ser311= | |
| XM_011529969.1:c.789G>C | XP_011528271.1:p.Ser263= | |
| XM_011529970.1:c.780G>C | XP_011528272.1:p.Ser260= | |
| XM_011529971.1:c.789G>C | XP_011528273.1:p.Ser263= | |
| XM_011529972.1:c.844-260G>C | XP_011528274.1:n.844-260G>C | |
| NM_000106.6:c.933G>C MANE Select | NP_000097.3:p.Ser311= | |
| NM_001025161.3:c.780G>C | NP_001020332.2:p.Ser260= |