Linked Data
MyVariant Identifiers:
chr16:g.23428317C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.23416996C>T , CM000678.2:g.23416996C>T | GRCh38 |
| NC_000016.9:g.23428317C>T , CM000678.1:g.23428317C>T | GRCh37 |
| NC_000016.8:g.23335818C>T | NCBI36 |
| NG_021287.1:g.41196G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000307149.10:c.1263G>A MANE Select | ENSP00000305442.5:p.Leu421= | |
| ENST00000307149.9:c.1263G>A | ENSP00000305442.5:p.Leu421= | |
| ENST00000567821.1:n.298G>A | ||
| NM_153603.3:c.1263G>A | NP_705831.1:p.Leu421= | |
| XR_429680.1:n.1479G>A | ||
| XM_017023870.1:c.1068G>A | XP_016879359.1:p.Leu356= | |
| XR_002957852.1:n.1484G>A | ||
| XR_429680.2:n.1484G>A | ||
| NM_153603.4:c.1263G>A MANE Select | NP_705831.1:p.Leu421= |