Linked Data
MyVariant Identifiers:
chr7:g.19156684C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.19117061C>G , CM000669.2:g.19117061C>G | GRCh38 |
| NC_000007.13:g.19156684C>G , CM000669.1:g.19156684C>G | GRCh37 |
| NC_000007.12:g.19123209C>G | NCBI36 |
| NG_008114.1:g.5612G>C | |
| NG_008114.2:g.5612G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000242261.6:c.261G>C MANE Select | ENSP00000242261.5:p.Ala87= | |
| ENST00000242261.5:c.261G>C | ENSP00000242261.5:p.Ala87= | |
| ENST00000354571.5:c.58G>C | ||
| NM_000474.3:c.261G>C | NP_000465.1:p.Ala87= | |
| XM_011515496.1:c.261G>C | XP_011513798.1:p.Ala87= | |
| NR_149001.1:n.612G>C | ||
| NM_000474.4:c.261G>C MANE Select | NP_000465.1:p.Ala87= | |
| NR_149001.2:n.576G>C |