Linked Data
dbSNP Id:
rs966551554
gnomAD v2:
6-6610680-G-T
gnomAD v3:
6-6610447-G-T
gnomAD v4:
6-6610447-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.6610447G>T , CM000668.2:g.6610447G>T | GRCh38 |
| NC_000006.11:g.6610680G>T , CM000668.1:g.6610680G>T | GRCh37 |
| NC_000006.10:g.6555679G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000230568.5:c.137-14479G>T (LY86) MANE Select | ENSP00000230568.3:n.137-14479G>T | |
| ENST00000230568.4:c.137-14479G>T (LY86) | ENSP00000230568.3:n.137-14479G>T | |
| ENST00000379953.6:c.137-14479G>T (LY86) | ENSP00000369286.1:n.137-14479G>T | |
| NM_004271.3:c.137-14479G>T (LY86) | NP_004262.1:n.137-14479G>T | |
| NR_026970.1:n.195+12185C>A (LY86-AS1) | ||
| XM_017011505.1:c.137-14479G>T (LY86) | XP_016866994.1:n.137-14479G>T | |
| NM_004271.4:c.137-14479G>T (LY86) MANE Select | NP_004262.1:n.137-14479G>T |