Canonical Allele Identifier: CA345505

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12813438G>A , CM000681.2:g.12813438G>A GRCh38
NC_000019.9:g.12924252G>A , CM000681.1:g.12924252G>A GRCh37
NC_000019.8:g.12785252G>A NCBI36
NG_012662.1:g.11825G>A , LRG_278:g.11825G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000221486.6:c.872G>A (RNASEH2A) MANE Select ENSP00000221486.4:p.Arg291His
ENST00000593017.2:n.1158G>A (RNASEH2A)
ENST00000639767.2:c.*751G>A (THSD8) ENSP00000491410.2:n.*751G>A
ENST00000643757.1:n.907G>A (RNASEH2A)
ENST00000221486.4:c.872G>A (RNASEH2A) ENSP00000221486.3:p.Arg291His
ENST00000589765.1:n.41+11740C>T (HOOK2)
ENST00000593017.1:n.1287G>A (RNASEH2A)
NM_006397.2:c.872G>A , LRG_278t1:c.872G>A (RNASEH2A) NP_006388.2:p.Arg291His
XM_006722619.2:c.740G>A (RNASEH2A) XP_006722682.1:p.Arg247His
NM_006397.3:c.872G>A (RNASEH2A) MANE Select NP_006388.2:p.Arg291His