MyVariant.info:
GRCh38
chr2:g.145043894T>G
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.145043894T>G , CM000664.2:g.145043894T>G | GRCh38 |
| NC_000002.11:g.145801461T>G , CM000664.1:g.145801461T>G | GRCh37 |
| NC_000002.10:g.145517931T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_033870.2:n.464-26926T>G | ||
| XR_923411.1:n.200+20621T>G | ||
| XR_923410.2:n.1051+20621T>G |