MyVariant.info:
GRCh38
chr5:g.151028379G>T
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.151028379G>T , CM000667.2:g.151028379G>T | GRCh38 |
| NC_000005.9:g.150407940G>T , CM000667.1:g.150407940G>T | GRCh37 |
| NC_000005.8:g.150388133G>T | NCBI36 |
| NG_030590.1:g.64282C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000388825.9:c.*249G>T MANE Select | ENSP00000373477.4:n.*249G>T | |
| ENST00000388825.8:c.*249G>T | ENSP00000373477.4:n.*249G>T | |
| ENST00000521632.1:c.739G>T | ||
| ENST00000614343.4:c.*711G>T | ENSP00000483660.1:n.*711G>T | |
| ENST00000622181.4:c.*249G>T | ENSP00000484258.1:n.*249G>T | |
| NM_002084.3:c.*249G>T | NP_002075.2:n.*249G>T | |
| NM_001329790.1:c.*249G>T | NP_001316719.1:n.*249G>T | |
| NM_002084.4:c.*249G>T | NP_002075.2:n.*249G>T | |
| NM_002084.5:c.*249G>T MANE Select | NP_002075.2:n.*249G>T | |
| NM_001329790.2:c.*249G>T | NP_001316719.1:n.*249G>T |