HGVS | Genome Assembly |
---|---|
NC_000004.12:g.87612036_87612041dup , CM000666.2:g.87612036_87612041dup | GRCh38 |
NC_000004.11:g.88533188_88533193dup , CM000666.1:g.88533188_88533193dup | GRCh37 |
NC_000004.10:g.88752212_88752217dup | NCBI36 |
NG_011595.1:g.8508_8513dup |
HGVS | Amino-acid change | |
---|---|---|
ENST00000651931.1:c.52-69_52-64dup MANE Select | ENSP00000498766.1:n.52-69_52-64dup | |
ENST00000282478.7:c.52-69_52-64dup | ENSP00000282478.7:n.52-69_52-64dup | |
ENST00000399271.5:c.52-69_52-64dup | ENSP00000382213.1:n.52-69_52-64dup | |
NM_014208.3:c.52-69_52-64dup MANE Select | NP_055023.2:n.52-69_52-64dup |