HGVS | Genome Assembly |
---|---|
NC_000007.14:g.5603522A>C , CM000669.2:g.5603522A>C | GRCh38 |
NC_000007.13:g.5643153A>C , CM000669.1:g.5643153A>C | GRCh37 |
NC_000007.12:g.5609679A>C | NCBI36 |
NG_030004.1:g.15718A>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000382361.8:c.1016A>C MANE Select | ENSP00000371798.3:p.Glu339Ala | |
ENST00000382361.7:c.1016A>C | ENSP00000371798.3:p.Glu339Ala | |
ENST00000405801.2:c.182A>C | ENSP00000383982.2:p.Glu61Ala | |
ENST00000444748.5:c.182A>C | ENSP00000404506.1:p.Glu61Ala | |
ENST00000447103.5:c.182A>C | ENSP00000409967.1:p.Glu61Ala | |
ENST00000473330.1:n.569A>C | ||
NM_003088.3:c.1016A>C | NP_003079.1:p.Glu339Ala | |
NM_003088.4:c.1016A>C MANE Select | NP_003079.1:p.Glu339Ala |