Linked Data
ClinVar Variation Id:
345091
ClinVar RCV Id:
RCV000300018
RCV000315344
RCV000335131
RCV000368862
RCV000370122
RCV000394005
RCV000401083
dbSNP Id:
rs546849670
gnomAD v2:
3-38590923-G-T
gnomAD v3:
3-38549432-G-T
gnomAD v4:
3-38549432-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.38549432G>T , CM000665.2:g.38549432G>T | GRCh38 |
| NC_000003.11:g.38590923G>T , CM000665.1:g.38590923G>T | GRCh37 |
| NC_000003.10:g.38565927G>T | NCBI36 |
| NG_008934.1:g.105241C>A , LRG_289:g.105241C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000327956.7:c.*889C>A | ENSP00000333674.7:n.*889C>A | |
| ENST00000333535.9:c.*889C>A | ENSP00000328968.4:n.*889C>A | |
| ENST00000413689.6:c.*889C>A MANE Plus Clinical | ENSP00000410257.1:n.*889C>A | |
| ENST00000423572.7:c.*889C>A MANE Select | ENSP00000398266.2:n.*889C>A | |
| ENST00000333535.8:c.*889C>A | ENSP00000328968.4:n.*889C>A | |
| ENST00000413689.5:c.*889C>A | ENSP00000410257.1:n.*889C>A | |
| ENST00000414099.6:c.*889C>A | ENSP00000398962.2:n.*889C>A | |
| ENST00000423572.6:c.*889C>A | ENSP00000398266.2:n.*889C>A | |
| ENST00000425664.5:c.*889C>A | ENSP00000416634.1:n.*889C>A | |
| ENST00000451551.6:c.*889C>A | ENSP00000388797.2:n.*889C>A | |
| ENST00000455624.6:c.*889C>A | ENSP00000399524.2:n.*889C>A | |
| NM_000335.4:c.*889C>A , LRG_289t2:c.*889C>A | NP_000326.2:n.*889C>A | |
| NM_001099404.1:c.*889C>A , LRG_289t3:c.*889C>A | NP_001092874.1:n.*889C>A | |
| NM_001099405.1:c.*889C>A | NP_001092875.1:n.*889C>A | |
| NM_001160160.1:c.*889C>A | NP_001153632.1:n.*889C>A | |
| NM_001160161.1:c.*889C>A | NP_001153633.1:n.*889C>A | |
| NM_198056.2:c.*889C>A , LRG_289t1:c.*889C>A | NP_932173.1:n.*889C>A | |
| XM_006713282.2:c.*889C>A | XP_006713345.1:n.*889C>A | |
| XM_011533991.1:c.*889C>A | XP_011532293.1:n.*889C>A | |
| XM_011533992.1:c.*889C>A | XP_011532294.1:n.*889C>A | |
| NM_001354701.1:c.*889C>A | NP_001341630.1:n.*889C>A | |
| XM_011533991.2:c.*889C>A | XP_011532293.1:n.*889C>A | |
| XM_017007017.1:c.*889C>A | XP_016862506.1:n.*889C>A | |
| NM_000335.5:c.*889C>A MANE Select | NP_000326.2:n.*889C>A | |
| NM_001160160.2:c.*889C>A | NP_001153632.1:n.*889C>A | |
| NM_001354701.2:c.*889C>A | NP_001341630.1:n.*889C>A | |
| NM_001099404.2:c.*889C>A MANE Plus Clinical | NP_001092874.1:n.*889C>A | |
| NM_001099405.2:c.*889C>A | NP_001092875.1:n.*889C>A | |
| NM_001160161.2:c.*889C>A | NP_001153633.1:n.*889C>A | |
| NM_198056.3:c.*889C>A | NP_932173.1:n.*889C>A |