HGVS | Genome Assembly |
---|---|
NC_000007.14:g.19117108_19117109insG , CM000669.2:g.19117108_19117109insG | GRCh38 |
NC_000007.13:g.19156731_19156732insG , CM000669.1:g.19156731_19156732insG | GRCh37 |
NC_000007.12:g.19123256_19123257insG | NCBI36 |
NG_008114.1:g.5564_5565insC | |
NG_008114.2:g.5564_5565insC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000242261.6:c.213_214insC MANE Select | ENSP00000242261.5:p.Gly72ArgfsTer? | |
ENST00000242261.5:c.213_214insC | ENSP00000242261.5:p.Gly72ArgfsTer? | |
ENST00000354571.5:c.10_11insC | ||
NM_000474.3:c.213_214insC | NP_000465.1:p.Gly72ArgfsTer? | |
XM_011515496.1:c.213_214insC | XP_011513798.1:p.Gly72ArgfsTer? | |
NR_149001.1:n.564_565insC | ||
NM_000474.4:c.213_214insC MANE Select | NP_000465.1:p.Gly72ArgfsTer? | |
NR_149001.2:n.528_529insC |