Linked Data
dbSNP Id:
rs1561609660
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.136046075G>C , CM000667.2:g.136046075G>C | GRCh38 |
| NC_000005.9:g.135381764G>C , CM000667.1:g.135381764G>C | GRCh37 |
| NC_000005.8:g.135409663G>C | NCBI36 |
| NG_012646.1:g.22181G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000442011.7:c.299-260G>C MANE Select | ENSP00000416330.2:n.299-260G>C | |
| ENST00000442011.6:c.299-260G>C | ENSP00000416330.2:n.299-260G>C | |
| ENST00000504185.5:n.456-260G>C | ||
| ENST00000506699.5:n.364-260G>C | ||
| ENST00000507018.5:c.216-260G>C | ||
| ENST00000515433.1:n.331G>C | ||
| NM_000358.2:c.299-260G>C | NP_000349.1:n.299-260G>C | |
| NM_000358.3:c.299-260G>C MANE Select | NP_000349.1:n.299-260G>C |