Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.35831372C>G , CM000681.2:g.35831372C>G | GRCh38 |
| NC_000019.9:g.36322274C>G , CM000681.1:g.36322274C>G | GRCh37 |
| NC_000019.8:g.41014114C>G | NCBI36 |
| NG_013356.2:g.42916G>C , LRG_693:g.42916G>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_004646.4:c.3312-1G>C MANE Select | NP_004637.1:n.3312-1G>C |
| ENST00000378910.10:c.3312-1G>C MANE Select | ENSP00000368190.4:n.3312-1G>C |
| NM_004646.3:c.3312-1G>C , LRG_693t1:c.3312-1G>C | NP_004637.1:n.3312-1G>C |
| ENST00000353632.6:c.3192-1G>C | ENSP00000343634.5:n.3192-1G>C |
| ENST00000378910.9:c.3312-1G>C | ENSP00000368190.4:n.3312-1G>C |