Canonical Allele Identifier: CA360289538
Gene: RASGRF2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.80502671T>A (hg19) chr5:g.81206852T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.81206852T>A , CM000667.2:g.81206852T>A GRCh38
NC_000005.9:g.80502671T>A , CM000667.1:g.80502671T>A GRCh37
NC_000005.8:g.80538427T>A NCBI36
NG_030334.1:g.251164T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000265080.9:c.2914T>A MANE Select ENSP00000265080.4:p.Ser972Thr
ENST00000265080.8:c.2914T>A ENSP00000265080.4:p.Ser972Thr
ENST00000503795.1:c.2914T>A ENSP00000421771.1:p.Ser972Thr
NM_006909.2:c.2914T>A NP_008840.1:p.Ser972Thr
XM_017009682.2:c.2629T>A XP_016865171.1:p.Ser877Thr
XR_002956166.1:n.3030T>A
NM_006909.3:c.2914T>A MANE Select NP_008840.1:p.Ser972Thr
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