HGVS | Genome Assembly |
---|---|
NC_000005.10:g.128300825T>G , CM000667.2:g.128300825T>G | GRCh38 |
NC_000005.9:g.127636517T>G , CM000667.1:g.127636517T>G | GRCh37 |
NC_000005.8:g.127664416T>G | NCBI36 |
NG_008750.1:g.242219A>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000703783.1:n.2942A>C | ||
ENST00000703785.1:n.2861A>C | ||
ENST00000262464.9:c.6158A>C MANE Select | ENSP00000262464.4:p.Asn2053Thr | |
ENST00000262464.8:c.6158A>C | ENSP00000262464.4:p.Asn2053Thr | |
ENST00000508053.5:c.6158A>C | ENSP00000424571.1:p.Asn2053Thr | |
ENST00000619499.4:c.6155A>C | ENSP00000482132.1:p.Asn2052Thr | |
NM_001999.3:c.6158A>C | NP_001990.2:p.Asn2053Thr | |
XM_017009228.2:c.6005A>C | XP_016864717.1:p.Asn2002Thr | |
NM_001999.4:c.6158A>C MANE Select | NP_001990.2:p.Asn2053Thr |