dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.44370393A>T , CM000672.2:g.44370393A>T | GRCh38 |
| NC_000010.10:g.44865841A>T , CM000672.1:g.44865841A>T | GRCh37 |
| NC_000010.9:g.44185847A>T | NCBI36 |
| NG_016861.1:g.19705T>A | |
| NG_016861.2:g.19705T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374429.6:c.*2935T>A | ENSP00000363551.2:n.*2935T>A | |
| NM_000609.6:c.*2935T>A | NP_000600.1:n.*2935T>A | |
| NM_001277990.1:c.*2495T>A | NP_001264919.1:n.*2495T>A | |
| XR_001747171.1:n.331+8244T>A | ||
| XR_001747172.1:n.331+8244T>A | ||
| XR_001747173.1:n.331+8244T>A | ||
| XR_001747174.1:n.331+8244T>A | ||
| NM_000609.7:c.*2935T>A | NP_000600.1:n.*2935T>A | |
| NM_001277990.2:c.*2495T>A | NP_001264919.1:n.*2495T>A |