Canonical Allele Identifier: CA403374096
Gene: RAX2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.3770675G>C (hg19) chr19:g.3770677G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3770677G>C , CM000681.2:g.3770677G>C GRCh38
NC_000019.9:g.3770675G>C , CM000681.1:g.3770675G>C GRCh37
NC_000019.8:g.3721675G>C NCBI36
NG_011565.1:g.6545C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000555633.3:c.499C>G MANE Select ENSP00000450456.3:p.Arg167Gly
ENST00000555633.2:c.499C>G ENSP00000450456.2:p.Arg167Gly
ENST00000555978.5:c.499C>G ENSP00000450687.2:p.Arg167Gly
NM_032753.3:c.499C>G NP_116142.1:p.Arg167Gly
XM_005259662.1:c.637C>G XP_005259719.1:p.Arg213Gly
NM_001319074.1:c.637C>G NP_001306003.1:p.Arg213Gly
NM_001319074.4:c.499C>G MANE Select NP_001306003.2:p.Arg167Gly
NM_032753.4:c.499C>G NP_116142.1:p.Arg167Gly
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