Canonical Allele Identifier: CA2674453186
Gene: RASGRF2 HGNC NCBI

Linked Data

gnomAD v4: 5-81207019-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.81207019T>C , CM000667.2:g.81207019T>C GRCh38
NC_000005.9:g.80502838T>C , CM000667.1:g.80502838T>C GRCh37
NC_000005.8:g.80538594T>C NCBI36
NG_030334.1:g.251331T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000265080.9:c.2967+114T>C MANE Select ENSP00000265080.4:n.2967+114T>C
ENST00000265080.8:c.2967+114T>C ENSP00000265080.4:n.2967+114T>C
ENST00000503795.1:c.2967+114T>C ENSP00000421771.1:n.2967+114T>C
NM_006909.2:c.2967+114T>C NP_008840.1:n.2967+114T>C
XM_017009682.2:c.2682+114T>C XP_016865171.1:n.2682+114T>C
XR_002956166.1:n.3083+114T>C
NM_006909.3:c.2967+114T>C MANE Select NP_008840.1:n.2967+114T>C
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