Canonical Allele Identifier: CA718009978
Gene: RMI2 HGNC NCBI

Linked Data

dbSNP Id: rs1164281508
MyVariant Identifiers: chr16:g.11403752C>T (hg19) chr16:g.11309895C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11309895C>T , CM000678.2:g.11309895C>T GRCh38
NC_000016.9:g.11403752C>T , CM000678.1:g.11403752C>T GRCh37
NC_000016.8:g.11311253C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000649869.1:n.152+60117C>T
ENST00000572173.1:c.-436-2934C>T ENSP00000461206.1:n.-436-2934C>T
ENST00000573910.1:n.161-6557C>T
XR_933070.1:n.733+60117C>T
XR_933070.3:n.876+60117C>T
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