Linked Data
dbSNP Id:
rs1397464862
gnomAD v4:
6-49459254-G-C
MyVariant Identifiers:
chr6:g.49426967G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.49459254G>C , CM000668.2:g.49459254G>C | GRCh38 |
| NC_000006.11:g.49426967G>C , CM000668.1:g.49426967G>C | GRCh37 |
| NC_000006.10:g.49534926G>C | NCBI36 |
| NG_007100.1:g.8886C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000274813.4:c.213C>G MANE Select | ENSP00000274813.3:p.Pro71= | |
| ENST00000274813.3:c.213C>G | ENSP00000274813.3:p.Pro71= | |
| NM_000255.3:c.213C>G | NP_000246.2:p.Pro71= | |
| XM_005249143.2:c.213C>G | XP_005249200.1:p.Pro71= | |
| XM_005249143.3:c.213C>G | XP_005249200.1:p.Pro71= | |
| NM_000255.4:c.213C>G MANE Select | NP_000246.2:p.Pro71= |