Linked Data
dbSNP Id:
rs759927155
ExAC:
19:6682047 G / A
gnomAD v2:
19-6682047-G-A
gnomAD v4:
19-6682036-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.6682036G>A , CM000681.2:g.6682036G>A | GRCh38 |
| NC_000019.9:g.6682047G>A , CM000681.1:g.6682047G>A | GRCh37 |
| NC_000019.8:g.6633047G>A | NCBI36 |
| NG_009557.1:g.43616C>T , LRG_27:g.43616C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695651.1:n.2609-6C>T | ||
| ENST00000695653.1:c.2170-6C>T | ENSP00000512084.1:n.2170-6C>T | |
| ENST00000695654.1:c.3286-6C>T | ENSP00000512085.1:n.3286-6C>T | |
| ENST00000695689.1:c.232-6C>T | ENSP00000512101.1:n.232-6C>T | |
| ENST00000695690.1:n.452-6C>T | ||
| ENST00000695691.1:n.452-6C>T | ||
| ENST00000245907.11:c.4261-6C>T MANE Select | ENSP00000245907.4:n.4261-6C>T | |
| ENST00000245907.10:c.4261-6C>T | ENSP00000245907.4:n.4261-6C>T | |
| ENST00000596548.1:c.382-6C>T | ENSP00000469744.1:n.382-6C>T | |
| ENST00000599899.5:n.1220-6C>T | ||
| ENST00000601008.1:c.242-4078C>T | ENSP00000471384.1:n.242-4078C>T | |
| NM_000064.3:c.4261-6C>T | NP_000055.2:n.4261-6C>T | |
| NM_000064.4:c.4261-6C>T MANE Select | NP_000055.2:n.4261-6C>T |