HGVS | Genome Assembly |
---|---|
NC_000006.12:g.32202914_32202919dup , CM000668.2:g.32202914_32202919dup | GRCh38 |
NC_000006.11:g.32170691_32170696dup , CM000668.1:g.32170691_32170696dup | GRCh37 |
NC_000006.10:g.32278669_32278674dup | NCBI36 |
NG_028190.1:g.26162_26167dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375023.3:c.3232-307_3232-302dup MANE Select | ENSP00000364163.3:n.3232-307_3232-302dup | |
ENST00000474612.1:n.1011_1016dup | ||
NM_004557.3:c.3232-307_3232-302dup | NP_004548.3:n.3232-307_3232-302dup | |
NR_134949.1:n.3472+864_3472+869dup | ||
NR_134950.1:n.3370+864_3370+869dup | ||
NM_004557.4:c.3232-307_3232-302dup MANE Select | NP_004548.3:n.3232-307_3232-302dup | |
NR_134949.2:n.3472+864_3472+869dup | ||
NR_134950.2:n.3370+864_3370+869dup |