Linked Data
MyVariant Identifiers:
chr4:g.3519810G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.3518083G>C , CM000666.2:g.3518083G>C | GRCh38 |
| NC_000004.11:g.3519810G>C , CM000666.1:g.3519810G>C | GRCh37 |
| NC_000004.10:g.3489608G>C | NCBI36 |
| NG_033873.1:g.19415C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000648517.1:c.702C>G | ENSP00000496947.1:p.Gly234= | |
| ENST00000650182.1:c.702C>G MANE Select | ENSP00000497444.1:p.Gly234= | |
| ENST00000296325.9:n.665C>G | ||
| ENST00000500728.2:c.702C>G | ENSP00000421922.1:p.Gly234= | |
| ENST00000509198.1:n.748C>G | ||
| ENST00000515119.5:c.*479C>G | ENSP00000421648.1:n.*479C>G | |
| NM_002337.3:c.702C>G | NP_002328.1:p.Gly234= | |
| NR_110005.1:n.665C>G | ||
| NM_002337.4:c.702C>G MANE Select | NP_002328.1:p.Gly234= | |
| XR_002959730.1:n.787C>G | ||
| NR_110005.2:n.665C>G |