Linked Data
MyVariant Identifiers:
chr7:g.141673169G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.141973369G>T , CM000669.2:g.141973369G>T | GRCh38 |
| NC_000007.13:g.141673169G>T , CM000669.1:g.141673169G>T | GRCh37 |
| NC_000007.12:g.141319638G>T | NCBI36 |
| NG_016141.1:g.5405C>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000465654.5:c.-3+27372G>T (MGAM) | ENSP00000419372.1:n.-3+27372G>T | |
| ENST00000547270.1:c.321C>A (TAS2R38) MANE Select | ENSP00000448219.1:p.Leu107= | |
| NM_176817.4:c.321C>A (TAS2R38) | NP_789787.4:p.Leu107= | |
| XM_011515783.1:c.*25-13027G>T (OR9A4) | XP_011514085.1:n.*25-13027G>T | |
| NM_176817.5:c.321C>A (TAS2R38) MANE Select | NP_789787.5:p.Leu107= |