HGVS | Genome Assembly |
---|---|
NC_000007.14:g.93104146G>A , CM000669.2:g.93104146G>A | GRCh38 |
NC_000007.13:g.92733459G>A , CM000669.1:g.92733459G>A | GRCh37 |
NC_000007.12:g.92571395G>A | NCBI36 |
NG_023419.1:g.18878C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000379958.3:c.1952C>T MANE Select | ENSP00000369292.2:p.Ala651Val | |
ENST00000379958.2:c.1952C>T | ENSP00000369292.2:p.Ala651Val | |
ENST00000446617.1:c.1952C>T | ENSP00000414529.1:p.Ala651Val | |
ENST00000620985.4:c.1952C>T | ENSP00000484636.1:p.Ala651Val | |
NM_001193307.1:c.1952C>T | NP_001180236.1:p.Ala651Val | |
NM_017654.3:c.1952C>T | NP_060124.2:p.Ala651Val | |
NM_017654.4:c.1952C>T MANE Select | NP_060124.2:p.Ala651Val | |
NM_001193307.2:c.1952C>T | NP_001180236.1:p.Ala651Val |