Linked Data
dbSNP Id:
rs963040655
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.160032876G>C , CM000668.2:g.160032876G>C | GRCh38 |
| NC_000006.11:g.160453908G>C , CM000668.1:g.160453908G>C | GRCh37 |
| NC_000006.10:g.160373898G>C | NCBI36 |
| NG_011785.3:g.68778G>C | |
| NG_011785.4:g.68778G>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000356956.6:c.1046-66G>C MANE Select | ENSP00000349437.1:n.1046-66G>C | |
| ENST00000649737.1:n.283-66G>C | ||
| ENST00000676781.1:c.1046-66G>C | ENSP00000504419.1:n.1046-66G>C | |
| ENST00000677704.1:c.1046-66G>C | ENSP00000503314.1:n.1046-66G>C | |
| ENST00000356956.5:c.1046-66G>C | ENSP00000349437.1:n.1046-66G>C | |
| NM_000876.2:c.1046-66G>C | NP_000867.2:n.1046-66G>C | |
| XR_942419.1:n.1061-66G>C | ||
| NM_000876.3:c.1046-66G>C | NP_000867.2:n.1046-66G>C | |
| NM_000876.4:c.1046-66G>C MANE Select | NP_000867.3:n.1046-66G>C |