Linked Data
gnomAD v4:
11-112086849-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.112086849G>A , CM000673.2:g.112086849G>A | GRCh38 |
| NC_000011.9:g.111957573G>A , CM000673.1:g.111957573G>A | GRCh37 |
| NC_000011.8:g.111462783G>A | NCBI36 |
| NG_012337.2:g.5003G>A | |
| NG_033145.1:g.4950C>T | |
| NG_012337.3:g.5003G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000640554.1:c.-59G>A | ENSP00000491141.1:n.-59G>A | |
| ENST00000375549.7:c.-59G>A | ENSP00000364699.3:n.-59G>A | |
| ENST00000614349.4:c.-59G>A | ENSP00000480666.1:n.-59G>A | |
| NM_001276503.1:c.-59G>A | NP_001263432.1:n.-59G>A | |
| NM_001276504.1:c.-59G>A | NP_001263433.1:n.-59G>A | |
| NM_001276506.1:c.-59G>A | NP_001263435.1:n.-59G>A | |
| NM_003002.3:c.-59G>A | NP_002993.1:n.-59G>A | |
| NR_077060.1:n.26G>A |