HGVS | Genome Assembly |
---|---|
NC_000012.12:g.12717271T>C , CM000674.2:g.12717271T>C | GRCh38 |
NC_000012.11:g.12870205T>C , CM000674.1:g.12870205T>C | GRCh37 |
NC_000012.10:g.12761472T>C | NCBI36 |
NG_016341.1:g.4904T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000682620.1:n.1631-1554T>C (CDKN1B) | ||
ENST00000684771.1:n.585-1554T>C (CDKN1B) | ||
ENST00000228872.8:c.-569T>C (CDKN1B) | ENSP00000228872.4:n.-569T>C | |
ENST00000477087.1:n.154+1388T>C (CDKN1B) | ||
NM_004064.4:c.-569T>C (CDKN1B) | NP_004055.1:n.-569T>C | |
XM_011520623.1:c.-1765A>G (GPR19) | XP_011518925.1:n.-1765A>G | |
XM_011520623.3:c.-1765A>G (GPR19) | XP_011518925.1:n.-1765A>G | |
XM_017019216.2:c.-1793A>G (GPR19) | XP_016874705.1:n.-1793A>G |