Linked Data
MyVariant Identifiers:
chr1:g.119683414C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.119140791C>G , CM000663.2:g.119140791C>G | GRCh38 |
| NC_000001.10:g.119683414C>G , CM000663.1:g.119683414C>G | GRCh37 |
| NC_000001.9:g.119484937C>G | NCBI36 |
| NG_050658.1:g.4998G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_125974.1:n.396C>G | ||
| NR_125975.1:n.396C>G | ||
| NR_125976.1:n.396C>G | ||
| NR_125977.1:n.396C>G |