Linked Data
dbSNP Id:
rs764920043
gnomAD v2:
10-8115686-A-C
gnomAD v3:
10-8073723-A-C
gnomAD v4:
10-8073723-A-C
MyVariant Identifiers:
chr10:g.8115686A>C (hg19)
chr10:g.8115686_8115687delinsCT (hg19)
chr10:g.8073723A>C (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.8073723A>C , CM000672.2:g.8073723A>C | GRCh38 |
| NC_000010.10:g.8115686A>C , CM000672.1:g.8115686A>C | GRCh37 |
| NC_000010.9:g.8155692A>C | NCBI36 |
| NG_015859.1:g.24020A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000346208.4:c.1048-16A>C | ENSP00000341619.3:n.1048-16A>C | |
| ENST00000379328.9:c.1051-16A>C MANE Select | ENSP00000368632.3:n.1051-16A>C | |
| ENST00000346208.3:c.1048-16A>C | ENSP00000341619.3:n.1048-16A>C | |
| ENST00000379328.7:c.1051-16A>C | ENSP00000368632.3:n.1051-16A>C | |
| ENST00000461472.1:n.570-16A>C | ||
| NM_001002295.1:c.1051-16A>C | NP_001002295.1:n.1051-16A>C | |
| NM_002051.2:c.1048-16A>C | NP_002042.1:n.1048-16A>C | |
| XM_005252442.2:c.1051-16A>C | XP_005252499.1:n.1051-16A>C | |
| XM_005252443.3:c.1051-16A>C | XP_005252500.1:n.1051-16A>C | |
| XM_005252443.5:c.1051-16A>C | XP_005252500.1:n.1051-16A>C | |
| NM_001002295.2:c.1051-16A>C MANE Select | NP_001002295.1:n.1051-16A>C | |
| NM_002051.3:c.1048-16A>C | NP_002042.1:n.1048-16A>C |