MyVariant.info:
GRCh38
chr6:g.96111973C>G
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.96111973C>G , CM000668.2:g.96111973C>G | GRCh38 |
| NC_000006.11:g.96559849C>G , CM000668.1:g.96559849C>G | GRCh37 |
| NC_000006.10:g.96666570C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000302103.6:c.-97-2066C>G MANE Select | ENSP00000302599.4:n.-97-2066C>G | |
| ENST00000302103.5:c.-97-2066C>G | ENSP00000302599.4:n.-97-2066C>G | |
| NM_006581.3:c.-97-2066C>G | NP_006572.2:n.-97-2066C>G | |
| XM_011535383.1:c.-98+1175C>G | XP_011533685.1:n.-98+1175C>G | |
| XM_011535384.1:c.-97-2066C>G | XP_011533686.1:n.-97-2066C>G | |
| XM_011535385.1:c.-215+1175C>G | XP_011533687.1:n.-215+1175C>G | |
| XM_011535383.2:c.-98+1175C>G | XP_011533685.1:n.-98+1175C>G | |
| XM_011535385.2:c.-215+1175C>G | XP_011533687.1:n.-215+1175C>G | |
| XM_017010188.1:c.-98+1175C>G | XP_016865677.1:n.-98+1175C>G | |
| XM_017010190.1:c.-214-2066C>G | XP_016865679.1:n.-214-2066C>G | |
| NM_006581.4:c.-97-2066C>G MANE Select | NP_006572.2:n.-97-2066C>G |