Linked Data
dbSNP Id:
rs1053335635
gnomAD v3:
6-6588969-G-A
gnomAD v4:
6-6588969-G-A
MyVariant Identifiers:
chr6:g.6588969G>A (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.6588969G>A , CM000668.2:g.6588969G>A | GRCh38 |
| NC_000006.11:g.6589202G>A , CM000668.1:g.6589202G>A | GRCh37 |
| NC_000006.10:g.6534201G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000230568.5:c.136+99G>A (LY86) MANE Select | ENSP00000230568.3:n.136+99G>A | |
| ENST00000230568.4:c.136+99G>A (LY86) | ENSP00000230568.3:n.136+99G>A | |
| ENST00000379953.6:c.136+99G>A (LY86) | ENSP00000369286.1:n.136+99G>A | |
| NM_004271.3:c.136+99G>A (LY86) | NP_004262.1:n.136+99G>A | |
| NR_026970.1:n.196-19480C>T (LY86-AS1) | ||
| XM_017011505.1:c.136+99G>A (LY86) | XP_016866994.1:n.136+99G>A | |
| NM_004271.4:c.136+99G>A (LY86) MANE Select | NP_004262.1:n.136+99G>A |