MyVariant.info:
GRCh37
chr5:g.88327782T>C
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.89031965T>C , CM000667.2:g.89031965T>C | GRCh38 |
| NC_000005.9:g.88327782T>C , CM000667.1:g.88327782T>C | GRCh37 |
| NC_000005.8:g.88363538T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_109941.1:n.498T>C | ||
| XR_948549.1:n.268+27781T>C | ||
| NR_136217.1:n.311-62994T>C | ||
| NR_136218.1:n.401-62994T>C | ||
| NR_136219.1:n.294-62994T>C | ||
| NR_136220.1:n.327-62994T>C | ||
| NR_136221.1:n.220-62994T>C | ||
| NR_136222.1:n.311-62994T>C |