Linked Data
MyVariant Identifiers:
chr17:g.41832884C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.43755516C>G , CM000679.2:g.43755516C>G | GRCh38 |
| NC_000017.10:g.41832884C>G , CM000679.1:g.41832884C>G | GRCh37 |
| NC_000017.9:g.39188410C>G | NCBI36 |
| NG_008078.2:g.8273G>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000301691.3:c.468G>C MANE Select | ENSP00000301691.1:p.Ala156= | |
| ENST00000301691.2:c.468G>C | ENSP00000301691.1:p.Ala156= | |
| NM_025237.2:c.468G>C | NP_079513.1:p.Ala156= | |
| NM_025237.3:c.468G>C MANE Select | NP_079513.1:p.Ala156= |