Linked Data
dbSNP Id:
rs1222454401
gnomAD v2:
2-241808507-T-C
gnomAD v3:
2-240869090-T-C
gnomAD v4:
2-240869090-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240869090T>C , CM000664.2:g.240869090T>C | GRCh38 |
| NC_000002.11:g.241808507T>C , CM000664.1:g.241808507T>C | GRCh37 |
| NC_000002.10:g.241457180T>C | NCBI36 |
| NG_008005.1:g.5346T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000307503.4:c.165+60T>C MANE Select | ENSP00000302620.3:n.165+60T>C | |
| ENST00000307503.3:c.165+60T>C | ENSP00000302620.3:n.165+60T>C | |
| ENST00000472436.1:n.185+60T>C | ||
| NM_000030.2:c.165+60T>C | NP_000021.1:n.165+60T>C | |
| XR_924060.1:n.405+1143A>G | ||
| NM_000030.3:c.165+60T>C MANE Select | NP_000021.1:n.165+60T>C |