Linked Data
MyVariant Identifiers:
chr8:g.23069651A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.23212138A>T , CM000670.2:g.23212138A>T | GRCh38 |
| NC_000008.10:g.23069651A>T , CM000670.1:g.23069651A>T | GRCh37 |
| NC_000008.9:g.23125596A>T | NCBI36 |
| NG_032107.1:g.18030T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000221132.8:c.381T>A MANE Select | ENSP00000221132.3:p.Pro127= | |
| ENST00000221132.7:c.381T>A | ENSP00000221132.3:p.Pro127= | |
| ENST00000524158.5:c.-226T>A | ENSP00000428884.1:n.-226T>A | |
| ENST00000613472.1:c.32-9479T>A | ENSP00000480778.1:n.32-9479T>A | |
| NM_003844.3:c.381T>A | NP_003835.3:p.Pro127= | |
| NM_003844.4:c.381T>A MANE Select | NP_003835.3:p.Pro127= |