Linked Data
dbSNP Id:
rs1442794443
gnomAD v2:
2-189858025-G-C
gnomAD v3:
2-188993299-G-C
gnomAD v4:
2-188993299-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.188993299G>C , CM000664.2:g.188993299G>C | GRCh38 |
| NC_000002.11:g.189858025G>C , CM000664.1:g.189858025G>C | GRCh37 |
| NC_000002.10:g.189566270G>C | NCBI36 |
| NG_007404.1:g.23927G>C , LRG_3:g.23927G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000450867.2:c.1050+359G>C | ENSP00000415346.2:n.1050+359G>C | |
| ENST00000304636.9:c.1051-62G>C MANE Select | ENSP00000304408.4:n.1051-62G>C | |
| ENST00000304636.7:c.1051-62G>C | ENSP00000304408.3:n.1051-62G>C | |
| ENST00000317840.9:c.1051-62G>C | ENSP00000315243.6:n.1051-62G>C | |
| ENST00000450867.1:c.148+359G>C | ||
| NM_000090.3:c.1051-62G>C , LRG_3t1:c.1051-62G>C | NP_000081.1:n.1051-62G>C | |
| NM_000090.4:c.1051-62G>C MANE Select | NP_000081.2:n.1051-62G>C |