Linked Data
dbSNP Id:
rs1018054486
gnomAD v2:
5-13692115-G-A
gnomAD v3:
5-13692006-G-A
gnomAD v4:
5-13692006-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.13692006G>A , CM000667.2:g.13692006G>A | GRCh38 |
| NC_000005.9:g.13692115G>A , CM000667.1:g.13692115G>A | GRCh37 |
| NC_000005.8:g.13745115G>A | NCBI36 |
| NG_013081.1:g.257475C>T | |
| NG_013081.2:g.257475C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000683611.1:n.1186C>T | ||
| ENST00000265104.5:c.13853C>T MANE Select | ENSP00000265104.4:p.Ala4618Val | |
| ENST00000681290.1:c.13808C>T | ENSP00000505288.1:p.Ala4603Val | |
| ENST00000265104.4:c.13853C>T | ENSP00000265104.4:p.Ala4618Val | |
| NM_001369.2:c.13853C>T | NP_001360.1:p.Ala4618Val | |
| XM_005248262.2:c.13808C>T | XP_005248319.1:p.Ala4603Val | |
| XM_005248262.3:c.13961C>T | XP_005248319.2:p.Ala4654Val | |
| XM_017009177.1:c.13541C>T | XP_016864666.1:p.Ala4514Val | |
| XM_017009178.1:c.12866C>T | XP_016864667.1:p.Ala4289Val | |
| XM_017009179.2:c.12866C>T | XP_016864668.1:p.Ala4289Val | |
| XM_017009185.1:c.9050C>T | XP_016864674.1:p.Ala3017Val | |
| XM_017009186.1:c.8603C>T | XP_016864675.1:p.Ala2868Val | |
| XM_017009188.1:c.7940C>T | XP_016864677.1:p.Ala2647Val | |
| XM_024454388.1:c.12866C>T | XP_024310156.1:p.Ala4289Val | |
| XM_024454389.1:c.12455C>T | XP_024310157.1:p.Ala4152Val | |
| NM_001369.3:c.13853C>T MANE Select | NP_001360.1:p.Ala4618Val |