Linked Data
dbSNP Id:
rs202076044
ExAC:
4:55976715 G / C
gnomAD v2:
4-55976715-G-C
gnomAD v4:
4-55110548-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.55110548G>C , CM000666.2:g.55110548G>C | GRCh38 |
| NC_000004.11:g.55976715G>C , CM000666.1:g.55976715G>C | GRCh37 |
| NC_000004.10:g.55671472G>C | NCBI36 |
| NG_012004.1:g.20048C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263923.5:c.1110C>G MANE Select | ENSP00000263923.4:p.Pro370= | |
| ENST00000647068.1:n.1123C>G | ||
| ENST00000263923.4:c.1110C>G | ENSP00000263923.4:p.Pro370= | |
| ENST00000512566.1:n.1110C>G | ||
| NM_002253.2:c.1110C>G | NP_002244.1:p.Pro370= | |
| NM_002253.3:c.1110C>G | NP_002244.1:p.Pro370= | |
| NM_002253.4:c.1110C>G MANE Select | NP_002244.1:p.Pro370= |