HGVS | Genome Assembly |
---|---|
NC_000005.10:g.139273924C>T , CM000667.2:g.139273924C>T | GRCh38 |
NC_000005.9:g.138609613C>T , CM000667.1:g.138609613C>T | GRCh37 |
NC_000005.8:g.138637512C>T | NCBI36 |
NG_012846.1:g.4822C>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000506147.5:c.-256C>T | ENSP00000423521.1:n.-256C>T | |
ENST00000508744.1:n.466-270G>A (SIL1) | ||
ENST00000509400.5:n.293+6644G>A (SIL1) | ||
ENST00000509990.5:c.-524C>T | ENSP00000423533.1:n.-524C>T | |
ENST00000512107.5:c.-473C>T | ENSP00000423695.1:n.-473C>T | |
NM_001194954.1:c.-524C>T (MATR3) | NP_001181883.1:n.-524C>T | |
NM_001282278.1:c.-531C>T (MATR3) | NP_001269207.1:n.-531C>T | |
NM_199189.2:c.-606C>T (MATR3) | NP_954659.1:n.-606C>T | |
NR_003141.3:n.173C>T (SNHG4) | ||
NR_036536.1:n.173C>T (SNHG4) |