HGVS | Genome Assembly |
---|---|
NC_000001.11:g.172664118T>C , CM000663.2:g.172664118T>C | GRCh38 |
NC_000001.10:g.172633258T>C , CM000663.1:g.172633258T>C | GRCh37 |
NC_000001.9:g.170899881T>C | NCBI36 |
NG_007269.1:g.10074T>C , LRG_58:g.10074T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367721.3:c.395-216T>C MANE Select | ENSP00000356694.2:n.395-216T>C | |
ENST00000340030.4:c.349-216T>C | ENSP00000344739.3:n.349-216T>C | |
ENST00000367721.2:c.395-216T>C | ENSP00000356694.2:n.395-216T>C | |
NM_000639.2:c.395-216T>C | NP_000630.1:n.395-216T>C | |
NM_001302746.1:c.349-216T>C | NP_001289675.1:n.349-216T>C | |
NM_000639.3:c.395-216T>C MANE Select | NP_000630.1:n.395-216T>C | |
NM_001302746.2:c.349-216T>C | NP_001289675.1:n.349-216T>C |