HGVS | Genome Assembly |
---|---|
NC_000009.12:g.97700127T>C , CM000671.2:g.97700127T>C | GRCh38 |
NC_000009.11:g.100462409T>C , CM000671.1:g.100462409T>C | GRCh37 |
NC_000009.10:g.99502230T>C | NCBI36 |
NG_011642.1:g.2283A>G , LRG_471:g.2283A>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000400056.3:n.683T>C (KRT18P13) | ||
NR_147055.1:n.1501-56A>G (PTCSC2) |