HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31861619C>G , CM000668.2:g.31861619C>G | GRCh38 |
NC_000006.11:g.31829396C>G , CM000668.1:g.31829396C>G | GRCh37 |
NC_000006.10:g.31937375C>G | NCBI36 |
NG_008201.1:g.6314G>C | |
NG_023058.1:g.22428G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375631.5:c.353-169G>C MANE Select | ENSP00000364782.4:n.353-169G>C | |
ENST00000677054.1:n.861G>C | ||
ENST00000677512.1:n.461-169G>C | ||
ENST00000678869.1:n.461-169G>C | ||
ENST00000375631.4:c.353-169G>C | ENSP00000364782.4:n.353-169G>C | |
ENST00000480384.1:n.382-169G>C | ||
ENST00000491768.5:c.353-169G>C | ENSP00000433127.1:n.353-169G>C | |
ENST00000495807.1:n.752G>C | ||
NM_000434.3:c.353-169G>C | NP_000425.1:n.353-169G>C | |
NM_000434.4:c.353-169G>C MANE Select | NP_000425.1:n.353-169G>C |