MyVariant.info:
GRCh37
chr1:g.226573364A>T
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.226385663A>T , CM000663.2:g.226385663A>T | GRCh38 |
| NC_000001.10:g.226573364A>T , CM000663.1:g.226573364A>T | GRCh37 |
| NC_000001.9:g.224639987A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000366794.10:c.852T>A MANE Select | ENSP00000355759.5:p.Ala284= | |
| ENST00000676685.1:n.1077T>A | ||
| ENST00000676709.1:n.1077T>A | ||
| ENST00000677091.1:c.852T>A | ENSP00000504745.1:p.Ala284= | |
| ENST00000677203.1:c.852T>A | ENSP00000503396.1:p.Ala284= | |
| ENST00000677374.1:n.1135T>A | ||
| ENST00000677884.1:n.1664T>A | ||
| ENST00000678144.1:c.852T>A | ENSP00000504430.1:p.Ala284= | |
| ENST00000678560.1:c.*840T>A | ENSP00000503293.1:n.*840T>A | |
| ENST00000678781.1:n.1077T>A | ||
| ENST00000679276.1:n.1077T>A | ||
| ENST00000366794.9:c.852T>A | ENSP00000355759.5:p.Ala284= | |
| NM_001618.3:c.852T>A | NP_001609.2:p.Ala284= | |
| NM_001618.4:c.852T>A MANE Select | NP_001609.2:p.Ala284= |