HGVS | Genome Assembly |
---|---|
NC_000005.10:g.128312630T>G , CM000667.2:g.128312630T>G | GRCh38 |
NC_000005.9:g.127648322T>G , CM000667.1:g.127648322T>G | GRCh37 |
NC_000005.8:g.127676221T>G | NCBI36 |
NG_008750.1:g.230414A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000703783.1:n.1663+4A>C | ||
ENST00000703785.1:n.1583-677A>C | ||
ENST00000262464.9:c.4879+4A>C MANE Select | ENSP00000262464.4:n.4879+4A>C | |
ENST00000262464.8:c.4879+4A>C | ENSP00000262464.4:n.4879+4A>C | |
ENST00000508053.5:c.4879+4A>C | ENSP00000424571.1:n.4879+4A>C | |
ENST00000619499.4:c.4876+4A>C | ENSP00000482132.1:n.4876+4A>C | |
NM_001999.3:c.4879+4A>C | NP_001990.2:n.4879+4A>C | |
XM_017009228.2:c.4726+4A>C | XP_016864717.1:n.4726+4A>C | |
NM_001999.4:c.4879+4A>C MANE Select | NP_001990.2:n.4879+4A>C |