Linked Data
MyVariant Identifiers:
chr7:g.19156873T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.19117250T>G , CM000669.2:g.19117250T>G | GRCh38 |
| NC_000007.13:g.19156873T>G , CM000669.1:g.19156873T>G | GRCh37 |
| NC_000007.12:g.19123398T>G | NCBI36 |
| NG_008114.1:g.5423A>C | |
| NG_008114.2:g.5423A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000242261.6:c.72A>C MANE Select | ENSP00000242261.5:p.Pro24= | |
| ENST00000242261.5:c.72A>C | ENSP00000242261.5:p.Pro24= | |
| NM_000474.3:c.72A>C | NP_000465.1:p.Pro24= | |
| XM_011515496.1:c.72A>C | XP_011513798.1:p.Pro24= | |
| NR_149001.1:n.423A>C | ||
| NM_000474.4:c.72A>C MANE Select | NP_000465.1:p.Pro24= | |
| NR_149001.2:n.387A>C |