Linked Data
dbSNP Id:
rs1575712190
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240877468A>C , CM000664.2:g.240877468A>C | GRCh38 |
| NC_000002.11:g.241816885A>C , CM000664.1:g.241816885A>C | GRCh37 |
| NC_000002.10:g.241465558A>C | NCBI36 |
| NG_008005.1:g.13724A>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000307503.4:c.847-69A>C MANE Select | ENSP00000302620.3:n.847-69A>C | |
| ENST00000307503.3:c.847-69A>C | ENSP00000302620.3:n.847-69A>C | |
| ENST00000470255.1:n.556A>C | ||
| NM_000030.2:c.847-69A>C | NP_000021.1:n.847-69A>C | |
| NM_000030.3:c.847-69A>C MANE Select | NP_000021.1:n.847-69A>C |