Linked Data
ClinVar Variation Id:
178748
dbSNP Id:
rs187023993
ExAC:
5:13820565 T / A
gnomAD v2:
5-13820565-T-A
gnomAD v3:
5-13820456-T-A
gnomAD v4:
5-13820456-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.13820456T>A , CM000667.2:g.13820456T>A | GRCh38 |
| NC_000005.9:g.13820565T>A , CM000667.1:g.13820565T>A | GRCh37 |
| NC_000005.8:g.13873565T>A | NCBI36 |
| NG_013081.1:g.129025A>T | |
| NG_013081.2:g.129025A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000683090.1:n.1662A>T | ||
| ENST00000265104.5:c.6731A>T MANE Select | ENSP00000265104.4:p.Lys2244Met | |
| ENST00000681290.1:c.6686A>T | ENSP00000505288.1:p.Lys2229Met | |
| ENST00000265104.4:c.6731A>T | ENSP00000265104.4:p.Lys2244Met | |
| NM_001369.2:c.6731A>T | NP_001360.1:p.Lys2244Met | |
| XM_005248262.2:c.6686A>T | XP_005248319.1:p.Lys2229Met | |
| XM_011513990.1:c.6731A>T | XP_011512292.1:p.Lys2244Met | |
| XR_925598.1:n.6938A>T | ||
| XM_005248262.3:c.6839A>T | XP_005248319.2:p.Lys2280Met | |
| XM_017009177.1:c.6839A>T | XP_016864666.1:p.Lys2280Met | |
| XM_017009178.1:c.5744A>T | XP_016864667.1:p.Lys1915Met | |
| XM_017009179.2:c.5744A>T | XP_016864668.1:p.Lys1915Met | |
| XM_017009180.1:c.6839A>T | XP_016864669.1:p.Lys2280Met | |
| XM_017009181.1:c.6839A>T | XP_016864670.1:p.Lys2280Met | |
| XM_017009182.1:c.6839A>T | XP_016864671.1:p.Lys2280Met | |
| XM_017009183.1:c.6839A>T | XP_016864672.1:p.Lys2280Met | |
| XM_017009184.1:c.6839A>T | XP_016864673.1:p.Lys2280Met | |
| XM_017009185.1:c.1928A>T | XP_016864674.1:p.Lys643Met | |
| XM_017009186.1:c.1481A>T | XP_016864675.1:p.Lys494Met | |
| XM_017009187.1:c.6839A>T | XP_016864676.1:p.Lys2280Met | |
| XM_017009188.1:c.818A>T | XP_016864677.1:p.Lys273Met | |
| XM_024454388.1:c.5744A>T | XP_024310156.1:p.Lys1915Met | |
| XM_024454389.1:c.5333A>T | XP_024310157.1:p.Lys1778Met | |
| XR_001742034.1:n.6856A>T | ||
| XR_001742035.1:n.6856A>T | ||
| NM_001369.3:c.6731A>T MANE Select | NP_001360.1:p.Lys2244Met |