HGVS | Genome Assembly |
---|---|
NC_000001.11:g.186453392A>T , CM000663.2:g.186453392A>T | GRCh38 |
NC_000001.10:g.186422524A>T , CM000663.1:g.186422524A>T | GRCh37 |
NC_000001.9:g.184689147A>T | NCBI36 |
NG_009101.1:g.12716T>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000391997.3:c.-24-3909T>A (PDC) MANE Select | ENSP00000375855.2:n.-24-3909T>A | |
ENST00000391997.2:c.-24-3909T>A (PDC) | ENSP00000375855.2:n.-24-3909T>A | |
NM_002597.4:c.-24-3909T>A (PDC) | NP_002588.3:n.-24-3909T>A | |
NR_126002.1:n.441+2118A>T (PDC-AS1) | ||
NM_002597.5:c.-24-3909T>A (PDC) MANE Select | NP_002588.3:n.-24-3909T>A |