HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154837682T>C , CM000685.2:g.154837682T>C | GRCh38 |
NC_000023.10:g.154065957T>C , CM000685.1:g.154065957T>C | GRCh37 |
NC_000023.9:g.153719151T>C | NCBI36 |
NG_011403.1:g.190042A>G | |
NG_033065.1:g.1981A>G | |
NG_011403.2:g.190042A>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000360256.9:c.6971A>G MANE Select | ENSP00000353393.4:p.Tyr2324Cys | |
ENST00000644698.1:c.704A>G | ENSP00000495706.1:p.Tyr235Cys | |
ENST00000330287.10:c.566A>G | ENSP00000327895.6:p.Tyr189Cys | |
ENST00000360256.8:c.6971A>G | ENSP00000353393.4:p.Tyr2324Cys | |
NM_000132.3:c.6971A>G | NP_000123.1:p.Tyr2324Cys | |
NM_019863.2:c.566A>G | NP_063916.1:p.Tyr189Cys | |
XM_011531126.1:c.6866A>G | XP_011529428.1:p.Tyr2289Cys | |
NM_000132.4:c.6971A>G MANE Select | NP_000123.1:p.Tyr2324Cys | |
NM_019863.3:c.566A>G | NP_063916.1:p.Tyr189Cys |