Linked Data
gnomAD v3:
1-40784162-A-C
gnomAD v4:
1-40784162-A-C
MyVariant Identifiers:
chr1:g.41249834A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.40784162A>C , CM000663.2:g.40784162A>C | GRCh38 |
| NC_000001.10:g.41249834A>C , CM000663.1:g.41249834A>C | GRCh37 |
| NC_000001.9:g.41022421A>C | NCBI36 |
| NG_008139.1:g.5151A>C | |
| NG_008139.2:g.5151A>C | |
| NG_008139.3:g.5376A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000347132.10:c.69A>C MANE Select | ENSP00000262916.6:p.Leu23= | |
| ENST00000347132.9:c.69A>C | ENSP00000262916.6:p.Leu23= | |
| ENST00000509682.6:c.69A>C | ENSP00000423756.2:p.Leu23= | |
| NM_004700.3:c.69A>C | NP_004691.2:p.Leu23= | |
| NM_172163.2:c.69A>C | NP_751895.1:p.Leu23= | |
| XM_011542417.1:c.69A>C | XP_011540719.1:p.Leu23= | |
| XM_011542418.1:c.69A>C | XP_011540720.1:p.Leu23= | |
| XM_011542419.1:c.69A>C | XP_011540721.1:p.Leu23= | |
| XM_011542420.1:c.69A>C | XP_011540722.1:p.Leu23= | |
| XR_946798.1:n.75A>C | ||
| XR_946799.1:n.75A>C | ||
| XR_946800.1:n.75A>C | ||
| NM_004700.4:c.69A>C MANE Select | NP_004691.2:p.Leu23= | |
| NM_172163.3:c.69A>C | NP_751895.1:p.Leu23= |