Canonical Allele Identifier: CA560571118
Gene: RASGRF2 HGNC NCBI

Linked Data

dbSNP Id: rs1482025353
gnomAD v2: 5-80502615-A-C
gnomAD v4: 5-81206796-A-C
MyVariant Identifiers: chr5:g.80502615A>C (hg19) chr5:g.81206796A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.81206796A>C , CM000667.2:g.81206796A>C GRCh38
NC_000005.9:g.80502615A>C , CM000667.1:g.80502615A>C GRCh37
NC_000005.8:g.80538371A>C NCBI36
NG_030334.1:g.251108A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000265080.9:c.2907-49A>C MANE Select ENSP00000265080.4:n.2907-49A>C
ENST00000265080.8:c.2907-49A>C ENSP00000265080.4:n.2907-49A>C
ENST00000503795.1:c.2907-49A>C ENSP00000421771.1:n.2907-49A>C
NM_006909.2:c.2907-49A>C NP_008840.1:n.2907-49A>C
XM_017009682.2:c.2622-49A>C XP_016865171.1:n.2622-49A>C
XR_002956166.1:n.3023-49A>C
NM_006909.3:c.2907-49A>C MANE Select NP_008840.1:n.2907-49A>C
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