Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.104037031C>G , CM000672.2:g.104037031C>G | GRCh38 |
| NC_000010.10:g.105796789C>G , CM000672.1:g.105796789C>G | GRCh37 |
| NC_000010.9:g.105786779C>G | NCBI36 |
| NG_007069.1:g.53850G>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000494.4:c.3277+14G>C MANE Select | NP_000485.3:n.3277+14G>C |
| ENST00000648076.2:c.3277+14G>C MANE Select | ENSP00000497653.1:n.3277+14G>C |
| NM_000494.3:c.3277+14G>C | NP_000485.3:n.3277+14G>C |
| ENST00000353479.9:c.3277+14G>C | ENSP00000340937.5:n.3277+14G>C |
| ENST00000369733.7:c.3142+14G>C | ENSP00000358748.3:n.3142+14G>C |
| ENST00000369733.8:c.3142+14G>C | ENSP00000358748.3:n.3142+14G>C |