Linked Data
dbSNP Id:
rs755643868
ExAC:
4:187201167 A / T
gnomAD v2:
4-187201167-A-T
gnomAD v4:
4-186280013-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.186280013A>T , CM000666.2:g.186280013A>T | GRCh38 |
| NC_000004.11:g.187201167A>T , CM000666.1:g.187201167A>T | GRCh37 |
| NC_000004.10:g.187438161A>T | NCBI36 |
| NG_008051.1:g.19050A>T , LRG_583:g.19050A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000403665.7:c.757A>T MANE Select | ENSP00000384957.2:p.Asn253Tyr | |
| ENST00000264692.8:c.595A>T | ENSP00000264692.5:p.Asn199Tyr | |
| ENST00000403665.6:c.757A>T | ENSP00000384957.2:p.Asn253Tyr | |
| ENST00000452239.1:c.204A>T | ||
| NM_000128.3:c.757A>T , LRG_583t1:c.757A>T | NP_000119.1:p.Asn253Tyr | |
| XM_005262821.2:c.757A>T | XP_005262878.1:p.Asn253Tyr | |
| XM_005262822.2:c.757A>T | XP_005262879.1:p.Asn253Tyr | |
| XM_005262823.2:c.487A>T | XP_005262880.1:p.Asn163Tyr | |
| XM_005262824.1:c.757A>T | XP_005262881.1:p.Asn253Tyr | |
| XM_006714137.1:c.757A>T | XP_006714200.1:p.Asn253Tyr | |
| XR_938706.1:n.1109A>T | ||
| XR_938707.1:n.1109A>T | ||
| XM_005262821.4:c.757A>T | XP_005262878.1:p.Asn253Tyr | |
| XM_005262822.4:c.757A>T | XP_005262879.1:p.Asn253Tyr | |
| XM_005262823.4:c.487A>T | XP_005262880.1:p.Asn163Tyr | |
| XM_006714137.3:c.757A>T | XP_006714200.1:p.Asn253Tyr | |
| XM_017007884.2:c.757A>T | XP_016863373.1:p.Asn253Tyr | |
| XM_017007885.2:c.757A>T | XP_016863374.1:p.Asn253Tyr | |
| XM_017007886.2:c.757A>T | XP_016863375.1:p.Asn253Tyr | |
| XR_001741172.2:n.1090A>T | ||
| NM_000128.4:c.757A>T MANE Select | NP_000119.1:p.Asn253Tyr |