HGVS | Genome Assembly |
---|---|
NC_000005.10:g.136056747A>T , CM000667.2:g.136056747A>T | GRCh38 |
NC_000005.9:g.135392436A>T , CM000667.1:g.135392436A>T | GRCh37 |
NC_000005.8:g.135420335A>T | NCBI36 |
NG_012646.1:g.32853A>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000442011.7:c.1630A>T MANE Select | ENSP00000416330.2:p.Asn544Tyr | |
ENST00000442011.6:c.1630A>T | ENSP00000416330.2:p.Asn544Tyr | |
ENST00000506699.5:n.2147A>T | ||
ENST00000507018.5:c.1608A>T | ||
ENST00000509485.5:c.627A>T | ||
ENST00000514242.5:n.401A>T | ||
ENST00000514554.5:c.782A>T | ||
NM_000358.2:c.1630A>T | NP_000349.1:p.Asn544Tyr | |
NM_000358.3:c.1630A>T MANE Select | NP_000349.1:p.Asn544Tyr |