Linked Data
dbSNP Id:
rs531513129
ExAC:
1:173878654 G / A
gnomAD v2:
1-173878654-G-A
gnomAD v3:
1-173909516-G-A
gnomAD v4:
1-173909516-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.173909516G>A , CM000663.2:g.173909516G>A | GRCh38 |
| NC_000001.10:g.173878654G>A , CM000663.1:g.173878654G>A | GRCh37 |
| NC_000001.9:g.172145277G>A | NCBI36 |
| NG_012462.1:g.12863C>T , LRG_577:g.12863C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367698.4:c.1153+36C>T MANE Select | ENSP00000356671.3:n.1153+36C>T | |
| ENST00000367698.3:c.1153+36C>T | ENSP00000356671.3:n.1153+36C>T | |
| ENST00000617423.4:c.560-2023C>T | ENSP00000478688.1:n.560-2023C>T | |
| NM_000488.3:c.1153+36C>T , LRG_577t1:c.1153+36C>T | NP_000479.1:n.1153+36C>T | |
| XM_005245198.2:c.1009+36C>T | XP_005245255.1:n.1009+36C>T | |
| NM_001365052.1:c.1009+36C>T | NP_001351981.1:n.1009+36C>T | |
| NM_000488.4:c.1153+36C>T MANE Select | NP_000479.1:n.1153+36C>T | |
| NM_001365052.2:c.1009+36C>T | NP_001351981.1:n.1009+36C>T | |
| NM_001386302.1:c.1276+36C>T | NP_001373231.1:n.1276+36C>T | |
| NM_001386303.1:c.1234+36C>T | NP_001373232.1:n.1234+36C>T | |
| NM_001386304.1:c.1132+36C>T | NP_001373233.1:n.1132+36C>T | |
| NM_001386305.1:c.1096+36C>T | NP_001373234.1:n.1096+36C>T | |
| NM_001386306.1:c.937+36C>T | NP_001373235.1:n.937+36C>T |