Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.37965509A>G , CM000670.2:g.37965509A>G | GRCh38 |
| NC_000008.10:g.37823027A>G , CM000670.1:g.37823027A>G | GRCh37 |
| NC_000008.9:g.37942184A>G | NCBI36 |
| NG_011936.1:g.6158T>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000025.3:c.961T>C MANE Select | NP_000016.1:p.Ser321Pro |
| ENST00000345060.5:c.961T>C MANE Select | ENSP00000343782.3:p.Ser321Pro |
| NM_000025.2:c.961T>C | NP_000016.1:p.Ser321Pro |
| ENST00000345060.4:c.961T>C | ENSP00000343782.3:p.Ser321Pro |
| ENST00000520341.1:n.236T>C | |
| ENST00000520341.2:n.1089T>C | |
| ENST00000614635.1:c.961T>C | ENSP00000480325.1:p.Ser321Pro |
| ENST00000647937.1:c.445T>C | ENSP00000497740.1:p.Ser149Pro |