Canonical Allele Identifier: CA632120906
Community Standard Title: NM_006397.3(RNASEH2A):c.550-13G>A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12810304G>A , CM000681.2:g.12810304G>A GRCh38
NC_000019.9:g.12921118G>A , CM000681.1:g.12921118G>A GRCh37
NC_000019.8:g.12782118G>A NCBI36
NG_012662.1:g.8691G>A , LRG_278:g.8691G>A

Transcript Alleles

HGVS Amino-acid Change
NM_006397.3:c.550-13G>A (RNASEH2A) MANE Select NP_006388.2:n.550-13G>A
ENST00000221486.6:c.550-13G>A (RNASEH2A) MANE Select ENSP00000221486.4:n.550-13G>A
NM_006397.2:c.550-13G>A , LRG_278t1:c.550-13G>A (RNASEH2A) NP_006388.2:n.550-13G>A
ENST00000221486.4:c.550-13G>A (RNASEH2A) ENSP00000221486.3:n.550-13G>A
ENST00000589765.1:n.41+14874C>T (HOOK2)
ENST00000593017.1:n.965-13G>A (RNASEH2A)
ENST00000593017.2:n.836-13G>A (RNASEH2A)
ENST00000639767.2:c.*429-13G>A (THSD8) ENSP00000491410.2:n.*429-13G>A
ENST00000643757.1:n.585-13G>A (RNASEH2A)
ENST00000646769.1:c.*210-13G>A (RNASEH2A) ENSP00000495175.1:n.*210-13G>A
XM_006722619.2:c.418-13G>A (RNASEH2A) XP_006722682.1:n.418-13G>A