Linked Data
dbSNP Id:
rs2046695072
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.120938505G>A , CM000671.2:g.120938505G>A | GRCh38 |
| NC_000009.11:g.123700783G>A , CM000671.1:g.123700783G>A | GRCh37 |
| NC_000009.10:g.122740604G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696279.1:c.5899-4551C>T | ||
| ENST00000696280.1:n.5668-4551C>T | ||
| ENST00000696281.1:c.*548-4551C>T | ENSP00000512521.1:n.*548-4551C>T | |
| ENST00000697921.1:n.4457-4551C>T | ||
| ENST00000697922.1:c.*5569-4551C>T | ENSP00000513478.1:n.*5569-4551C>T |