HGVS | Genome Assembly |
---|---|
NC_000011.10:g.112086839C>A , CM000673.2:g.112086839C>A | GRCh38 |
NC_000011.9:g.111957563C>A , CM000673.1:g.111957563C>A | GRCh37 |
NC_000011.8:g.111462773C>A | NCBI36 |
NG_012337.2:g.4993C>A | |
NG_033145.1:g.4960G>T | |
NG_012337.3:g.4993C>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000640554.1:c.-69C>A | ENSP00000491141.1:n.-69C>A | |
ENST00000375549.7:c.-69C>A | ENSP00000364699.3:n.-69C>A | |
ENST00000614349.4:c.-69C>A | ENSP00000480666.1:n.-69C>A | |
NM_001276503.1:c.-69C>A | NP_001263432.1:n.-69C>A | |
NM_001276504.1:c.-69C>A | NP_001263433.1:n.-69C>A | |
NM_001276506.1:c.-69C>A | NP_001263435.1:n.-69C>A | |
NM_003002.3:c.-69C>A | NP_002993.1:n.-69C>A | |
NR_077060.1:n.16C>A |