HGVS | Genome Assembly |
---|---|
NC_000005.10:g.174724974G>T , CM000667.2:g.174724974G>T | GRCh38 |
NC_000005.9:g.174151977G>T , CM000667.1:g.174151977G>T | GRCh37 |
NC_000005.8:g.174084583G>T | NCBI36 |
NG_008124.1:g.5403G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000239243.7:c.315G>T MANE Select | ENSP00000239243.5:p.Lys105Asn | |
ENST00000239243.6:c.315G>T | ENSP00000239243.5:p.Lys105Asn | |
ENST00000507785.2:c.315G>T | ENSP00000427425.1:p.Lys105Asn | |
NM_002449.4:c.315G>T | NP_002440.2:p.Lys105Asn | |
NM_001363626.1:c.315G>T | NP_001350555.1:p.Lys105Asn | |
NM_002449.5:c.315G>T MANE Select | NP_002440.2:p.Lys105Asn | |
NM_001363626.2:c.315G>T | NP_001350555.1:p.Lys105Asn |