Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.26927965A>G , CM000667.2:g.26927965A>G | GRCh38 |
| NC_000005.9:g.26928073A>G , CM000667.1:g.26928073A>G | GRCh37 |
| NC_000005.8:g.26963830A>G | NCBI36 |
| NG_046968.1:g.198234T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000231021.9:c.229-12041T>C MANE Select | ENSP00000231021.4:n.229-12041T>C | |
| ENST00000231021.8:c.229-12041T>C | ENSP00000231021.4:n.229-12041T>C | |
| ENST00000505045.1:n.402-12041T>C | ||
| ENST00000511822.1:c.229-12041T>C | ENSP00000422538.1:n.229-12041T>C | |
| ENST00000513289.5:c.229-12041T>C | ENSP00000426239.1:n.229-12041T>C | |
| NM_016279.3:c.229-12041T>C | NP_057363.3:n.229-12041T>C | |
| XM_011513922.1:c.229-12041T>C | XP_011512224.1:n.229-12041T>C | |
| NM_016279.4:c.229-12041T>C MANE Select | NP_057363.3:n.229-12041T>C |