MyVariant.info:
GRCh37
chr1:g.145507646G>C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.145927447C>G , CM000663.2:g.145927447C>G | GRCh38 |
| NC_000001.10:g.145507646G>C , CM000663.1:g.145507646G>C | GRCh37 |
| NC_000001.9:g.144219003G>C | NCBI36 |
| NG_032654.2:g.5090G>C , LRG_574:g.5090G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000691760.1:c.-21G>C (RBM8A) | ENSP00000510519.1:n.-21G>C | |
| ENST00000692065.1:n.18G>C (RBM8A) | ||
| ENST00000583313.7:c.-21G>C (RBM8A) MANE Select | ENSP00000463058.2:n.-21G>C | |
| ENST00000369307.4:c.-21G>C (RBM8A) | ENSP00000358313.3:n.-21G>C | |
| ENST00000484825.1:n.49G>C (RBM8A) | ||
| ENST00000498663.5:n.49G>C (RBM8A) | ||
| ENST00000583313.6:c.-21G>C (RBM8A) | ENSP00000463058.1:n.-21G>C | |
| ENST00000625258.1:c.-30+158C>G | ENSP00000487094.1:n.-30+158C>G | |
| ENST00000630636.1:n.190C>G | ||
| ENST00000632555.1:c.-21G>C (RBM8A) | ENSP00000488265.1:n.-21G>C | |
| ENST00000634161.1:n.116G>C (RBM8A) | ||
| NM_005105.4:c.-21G>C , LRG_574t1:c.-21G>C (RBM8A) | NP_005096.1:n.-21G>C | |
| NR_147182.1:n.500C>G (LIX1L-AS1) | ||
| NM_005105.5:c.-21G>C (RBM8A) MANE Select | NP_005096.1:n.-21G>C |