MyVariant.info:
GRCh38
chr17:g.45727828T>C
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.45727828T>C , CM000679.2:g.45727828T>C | GRCh38 |
| NC_000017.10:g.43805194T>C , CM000679.1:g.43805194T>C | GRCh37 |
| NC_000017.9:g.41160977T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000587305.1:n.447+54926T>C | ||
| ENST00000634540.1:c.-492-79182T>C | ENSP00000488912.1:n.-492-79182T>C | |
| NM_001256299.2:c.-492-79182T>C | NP_001243228.1:n.-492-79182T>C | |
| NM_001303016.1:c.-185+54926T>C | NP_001289945.1:n.-185+54926T>C | |
| NM_001256299.3:c.-492-79182T>C | NP_001243228.1:n.-492-79182T>C |