MyVariant.info:
GRCh37
chr3:g.128190941C>T
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.128472098C>T , CM000665.2:g.128472098C>T | GRCh38 |
| NC_000003.11:g.128190941C>T , CM000665.1:g.128190941C>T | GRCh37 |
| NC_000003.10:g.129673631C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_037890.1:n.1579C>T |