Linked Data
MyVariant Identifiers:
chr7:g.19156408A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.19116785A>C , CM000669.2:g.19116785A>C | GRCh38 |
| NC_000007.13:g.19156408A>C , CM000669.1:g.19156408A>C | GRCh37 |
| NC_000007.12:g.19122933A>C | NCBI36 |
| NG_008114.1:g.5888T>G | |
| NG_008114.2:g.5888T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000242261.6:c.537T>G MANE Select | ENSP00000242261.5:p.Ala179= | |
| ENST00000242261.5:c.537T>G | ENSP00000242261.5:p.Ala179= | |
| ENST00000354571.5:c.334T>G | ||
| ENST00000443687.5:c.140T>G | ||
| NM_000474.3:c.537T>G | NP_000465.1:p.Ala179= | |
| XM_011515496.1:c.537T>G | XP_011513798.1:p.Ala179= | |
| NR_149001.1:n.888T>G | ||
| NM_000474.4:c.537T>G MANE Select | NP_000465.1:p.Ala179= | |
| NR_149001.2:n.852T>G |