Canonical Allele Identifier: CA853937320
Gene: ERICH1 HGNC NCBI

Linked Data

dbSNP Id: rs1232120307
MyVariant Identifiers: chr8:g.566043A>C (hg19) chr8:g.616043A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.616043A>C , CM000670.2:g.616043A>C GRCh38
NC_000008.10:g.566043A>C , CM000670.1:g.566043A>C GRCh37
NC_000008.9:g.556043A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000522706.5:c.977-759T>G ENSP00000428635.1:n.977-759T>G
ENST00000523415.5:c.2336T>G
NM_001303100.1:c.*528T>G NP_001290029.1:n.*528T>G
XM_011534732.1:c.1442-759T>G XP_011533034.1:n.1442-759T>G
XM_011534735.1:c.*1963T>G XP_011533037.1:n.*1963T>G
XM_011534735.3:c.*1963T>G XP_011533037.1:n.*1963T>G
XM_017013124.2:c.1457-759T>G XP_016868613.1:n.1457-759T>G
NM_001303100.2:c.*528T>G NP_001290029.1:n.*528T>G
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