HGVS | Genome Assembly |
---|---|
NC_000007.14:g.93103867G>T , CM000669.2:g.93103867G>T | GRCh38 |
NC_000007.13:g.92733180G>T , CM000669.1:g.92733180G>T | GRCh37 |
NC_000007.12:g.92571116G>T | NCBI36 |
NG_023419.1:g.19157C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000379958.3:c.2231C>A MANE Select | ENSP00000369292.2:p.Thr744Asn | |
ENST00000379958.2:c.2231C>A | ENSP00000369292.2:p.Thr744Asn | |
ENST00000446617.1:c.2231C>A | ENSP00000414529.1:p.Thr744Asn | |
ENST00000620985.4:c.2231C>A | ENSP00000484636.1:p.Thr744Asn | |
NM_001193307.1:c.2231C>A | NP_001180236.1:p.Thr744Asn | |
NM_017654.3:c.2231C>A | NP_060124.2:p.Thr744Asn | |
NM_017654.4:c.2231C>A MANE Select | NP_060124.2:p.Thr744Asn | |
NM_001193307.2:c.2231C>A | NP_001180236.1:p.Thr744Asn |