Linked Data
dbSNP Id:
rs1024094120
gnomAD v4:
6-121446728-C-A
MyVariant Identifiers:
chr6:g.121446728C>A (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.121446728C>A , CM000668.2:g.121446728C>A | GRCh38 |
| NC_000006.11:g.121767874C>A , CM000668.1:g.121767874C>A | GRCh37 |
| NC_000006.10:g.121809573C>A | NCBI36 |
| NG_008308.1:g.16130C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000282561.4:c.-16-104C>A MANE Select | ENSP00000282561.3:n.-16-104C>A | |
| ENST00000647564.1:c.-16-104C>A | ENSP00000497565.1:n.-16-104C>A | |
| ENST00000649003.1:c.-16-104C>A | ENSP00000497283.1:n.-16-104C>A | |
| ENST00000650427.1:c.-16-104C>A | ENSP00000497367.1:n.-16-104C>A | |
| ENST00000282561.3:c.-16-104C>A | ENSP00000282561.3:n.-16-104C>A | |
| NM_000165.4:c.-16-104C>A | NP_000156.1:n.-16-104C>A | |
| NM_000165.5:c.-16-104C>A MANE Select | NP_000156.1:n.-16-104C>A |