Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.80665223C>T , CM000667.2:g.80665223C>T | GRCh38 |
| NC_000005.9:g.79961042C>T , CM000667.1:g.79961042C>T | GRCh37 |
| NC_000005.8:g.79996798C>T | NCBI36 |
| NG_016607.1:g.15749C>T | |
| NG_016607.2:g.15749C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_002439.5:c.439C>T MANE Select | NP_002430.3:p.Pro147Ser |
| ENST00000265081.7:c.439C>T MANE Select | ENSP00000265081.6:p.Pro147Ser |
| NM_002439.4:c.439C>T | NP_002430.3:p.Pro147Ser |
| ENST00000265081.6:c.439C>T | ENSP00000265081.6:p.Pro147Ser |
| ENST00000658259.1:c.271C>T | ENSP00000499617.1:p.Pro91Ser |
| ENST00000667069.1:c.439C>T | ENSP00000499502.1:p.Pro147Ser |
| ENST00000670357.1:c.439C>T | ENSP00000499791.1:p.Pro147Ser |