HGVS | Genome Assembly |
---|---|
NC_000004.12:g.55096429_55096430dup , CM000666.2:g.55096429_55096430dup | GRCh38 |
NC_000004.11:g.55962596_55962597dup , CM000666.1:g.55962596_55962597dup | GRCh37 |
NC_000004.10:g.55657353_55657354dup | NCBI36 |
NG_012004.1:g.34167_34168dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000263923.5:c.2615-87_2615-86dup MANE Select | ENSP00000263923.4:n.2615-87_2615-86dup | |
ENST00000647068.1:n.2628-87_2628-86dup | ||
ENST00000263923.4:c.2615-87_2615-86dup | ENSP00000263923.4:n.2615-87_2615-86dup | |
ENST00000509309.1:n.292_293dup | ||
NM_002253.2:c.2615-87_2615-86dup | NP_002244.1:n.2615-87_2615-86dup | |
NM_002253.3:c.2615-87_2615-86dup | NP_002244.1:n.2615-87_2615-86dup | |
NM_002253.4:c.2615-87_2615-86dup MANE Select | NP_002244.1:n.2615-87_2615-86dup |