Linked Data
dbSNP Id:
rs1699504030
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.37562557C>T , CM000665.2:g.37562557C>T | GRCh38 |
| NC_000003.11:g.37604048C>T , CM000665.1:g.37604048C>T | GRCh37 |
| NC_000003.10:g.37579052C>T | NCBI36 |
| NG_016166.1:g.115236C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264741.10:c.1689+19972C>T MANE Select | ENSP00000264741.5:n.1689+19972C>T | |
| ENST00000264741.9:c.1689+19972C>T | ENSP00000264741.5:n.1689+19972C>T | |
| ENST00000422441.5:c.1689+19972C>T | ENSP00000397258.1:n.1689+19972C>T | |
| NM_002207.2:c.1689+19972C>T | NP_002198.2:n.1689+19972C>T | |
| NM_002207.3:c.1689+19972C>T MANE Select | NP_002198.2:n.1689+19972C>T |