Linked Data
gnomAD v4:
10-104037925-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.104037925G>C , CM000672.2:g.104037925G>C | GRCh38 |
| NC_000010.10:g.105797683G>C , CM000672.1:g.105797683G>C | GRCh37 |
| NC_000010.9:g.105787673G>C | NCBI36 |
| NG_007069.1:g.52956C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369733.8:c.2936-152C>G | ENSP00000358748.3:n.2936-152C>G | |
| ENST00000648076.2:c.3071-152C>G MANE Select | ENSP00000497653.1:n.3071-152C>G | |
| ENST00000353479.9:c.3071-152C>G | ENSP00000340937.5:n.3071-152C>G | |
| ENST00000369733.7:c.2936-152C>G | ENSP00000358748.3:n.2936-152C>G | |
| NM_000494.3:c.3071-152C>G | NP_000485.3:n.3071-152C>G | |
| NM_000494.4:c.3071-152C>G MANE Select | NP_000485.3:n.3071-152C>G |