Linked Data
dbSNP Id:
rs1803406163
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.141973557_141973558insACCTTCCTGA , CM000669.2:g.141973557_141973558insACCTTCCTGA | GRCh38 |
| NC_000007.13:g.141673357_141673358insACCTTCCTGA , CM000669.1:g.141673357_141673358insACCTTCCTGA | GRCh37 |
| NC_000007.12:g.141319826_141319827insACCTTCCTGA | NCBI36 |
| NG_016141.1:g.5216_5217insTCAGGAAGGT |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000465654.5:c.-3+27560_-3+27561insACCTTCCTGA (MGAM) | ENSP00000419372.1:n.-3+27560_-3+27561insA... | |
| ENST00000547270.1:c.132_133insTCAGGAAGGT (TAS2R38) MANE Select | ENSP00000448219.1:p.Val45SerfsTer13 | |
| NM_176817.4:c.132_133insTCAGGAAGGT (TAS2R38) | NP_789787.4:p.Val45SerfsTer13 | |
| XM_011515783.1:c.*25-12839_*25-12838insACCTTCCTGA (OR9A4) | XP_011514085.1:n.*25-12839_*25-12838insAC... | |
| NM_176817.5:c.132_133insTCAGGAAGGT (TAS2R38) MANE Select | NP_789787.5:p.Val45SerfsTer13 |