Linked Data
dbSNP Id:
rs1049078674
gnomAD v2:
16-2390729-T-C
gnomAD v3:
16-2340728-T-C
gnomAD v4:
16-2340728-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.2340728T>C , CM000678.2:g.2340728T>C | GRCh38 |
| NC_000016.9:g.2390729T>C , CM000678.1:g.2390729T>C | GRCh37 |
| NC_000016.8:g.2330730T>C | NCBI36 |
| NG_011790.1:g.5019A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000301732.10:c.-694A>G (ABCA3) MANE Select | ENSP00000301732.5:n.-694A>G | |
| ENST00000640929.1:n.42+1397T>C (ABCA17P) | ||
| ENST00000301732.9:c.-694A>G (ABCA3) | ENSP00000301732.5:n.-694A>G | |
| ENST00000382381.7:c.-694A>G (ABCA3) | ENSP00000371818.3:n.-694A>G | |
| ENST00000512848.5:n.182+1397T>C (ABCA17P) | ||
| NM_001089.2:c.-694A>G (ABCA3) | NP_001080.2:n.-694A>G | |
| NM_001089.3:c.-694A>G (ABCA3) MANE Select | NP_001080.2:n.-694A>G |