Linked Data
gnomAD v4:
5-34008111-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.34008111G>A , CM000667.2:g.34008111G>A | GRCh38 |
| NC_000005.9:g.34008216G>A , CM000667.1:g.34008216G>A | GRCh37 |
| NC_000005.8:g.34043973G>A | NCBI36 |
| NG_016211.1:g.5005C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382079.3:c.690-2212C>T (C1QTNF3-AMACR) | ENSP00000371511.3:n.690-2212C>T | |
| NM_001167595.1:c.-92C>T (AMACR) | NP_001161067.1:n.-92C>T | |
| NM_014324.5:c.-92C>T (AMACR) | NP_055139.4:n.-92C>T | |
| NM_203382.2:c.-92C>T (AMACR) | NP_976316.1:n.-92C>T | |
| NR_037951.1:n.765-2212C>T (C1QTNF3-AMACR) |