HGVS | Genome Assembly |
---|---|
NC_000009.12:g.119222275A>T , CM000671.2:g.119222275A>T | GRCh38 |
NC_000009.11:g.121984553A>T , CM000671.1:g.121984553A>T | GRCh37 |
NC_000009.10:g.121024374A>T | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000265922.8:c.686-8120T>A MANE Select | ENSP00000265922.2:n.686-8120T>A | |
ENST00000265922.7:c.686-8120T>A | ENSP00000265922.2:n.686-8120T>A | |
ENST00000373964.2:c.686-8120T>A | ENSP00000363075.1:n.686-8120T>A | |
NM_014618.2:c.686-8120T>A | NP_055433.2:n.686-8120T>A | |
NM_014618.3:c.686-8120T>A MANE Select | NP_055433.2:n.686-8120T>A |