Linked Data
MyVariant Identifiers:
chr16:g.17232429C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.17138572C>T , CM000678.2:g.17138572C>T | GRCh38 |
| NC_000016.9:g.17232429C>T , CM000678.1:g.17232429C>T | GRCh37 |
| NC_000016.8:g.17139930C>T | NCBI36 |
| NG_015843.1:g.337310G>A | |
| NG_015843.2:g.337310G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261381.7:c.1588-41G>A MANE Select | ENSP00000261381.6:n.1588-41G>A | |
| ENST00000261381.6:c.1588-41G>A | ENSP00000261381.6:n.1588-41G>A | |
| NM_022166.3:c.1588-41G>A | NP_071449.1:n.1588-41G>A | |
| XM_011522574.1:c.1588-41G>A | XP_011520876.1:n.1588-41G>A | |
| XR_933141.1:n.505C>T | ||
| NR_135179.1:n.477C>T | ||
| XM_017023539.2:c.1588-41G>A | XP_016879028.1:n.1588-41G>A | |
| XM_017023540.2:c.1588-41G>A | XP_016879029.1:n.1588-41G>A | |
| NM_022166.4:c.1588-41G>A MANE Select | NP_071449.1:n.1588-41G>A |