Linked Data
dbSNP Id:
rs1461752524
gnomAD v4:
15-34790439-T-G
MyVariant Identifiers:
chr15:g.35082640T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.34790439T>G , CM000677.2:g.34790439T>G | GRCh38 |
| NC_000015.9:g.35082640T>G , CM000677.1:g.35082640T>G | GRCh37 |
| NC_000015.8:g.32869932T>G | NCBI36 |
| NG_007553.1:g.10288A>C , LRG_388:g.10288A>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000560563.2:n.2007A>C (ACTC1) | ||
| ENST00000290378.6:c.1107A>C (ACTC1) MANE Select | ENSP00000290378.4:p.Pro369= | |
| ENST00000647798.1:n.1201A>C (ACTC1) | ||
| ENST00000650163.1:n.1187A>C (ACTC1) | ||
| ENST00000290378.4:c.1107A>C (ACTC1) | ENSP00000290378.4:p.Pro369= | |
| NM_005159.4:c.1107A>C , LRG_388t1:c.1107A>C (ACTC1) | NP_005150.1:p.Pro369= | |
| NR_120329.1:n.299+13008T>G (GJD2-DT) | ||
| NM_005159.5:c.1107A>C (ACTC1) MANE Select | NP_005150.1:p.Pro369= |