HGVS | Genome Assembly |
---|---|
NC_000009.12:g.133256320C>A , CM000671.2:g.133256320C>A | GRCh38 |
NC_000009.11:g.136131707C>A , CM000671.1:g.136131707C>A | GRCh37 |
NC_000009.10:g.135121528C>A | NCBI36 |
NG_006669.1:g.21348G>T | |
NG_006669.2:g.23896G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000453660.4:n.440G>T | ||
ENST00000647353.1:n.54-5168G>T | ||
ENST00000651471.1:n.366G>T | ||
ENST00000679909.1:c.28+18842G>T | ENSP00000506089.1:n.28+18842G>T | |
ENST00000453660.3:n.422G>T | ||
ENST00000538324.2:c.408G>T | ENSP00000483018.1:p.Ala136= | |
ENST00000611156.4:c.408G>T | ENSP00000483265.1:p.Ala136= | |
NM_020469.2:c.411G>T | NP_065202.2:p.Ala137= | |
NM_020469.3:c.411G>T | NP_065202.2:p.Ala137= |