Canonical Allele Identifier: CA2175727370
Gene: SHC4 HGNC NCBI

Linked Data

dbSNP Id: rs1595761166

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48929318T>G , CM000677.2:g.48929318T>G GRCh38
NC_000015.9:g.49221515T>G , CM000677.1:g.49221515T>G GRCh37
NC_000015.8:g.47008807T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000332408.9:c.586-4369A>C MANE Select ENSP00000329668.4:n.586-4369A>C
ENST00000332408.8:c.586-4369A>C ENSP00000329668.4:n.586-4369A>C
NM_203349.3:c.586-4369A>C NP_976224.3:n.586-4369A>C
XM_005254375.2:c.37-4369A>C XP_005254432.1:n.37-4369A>C
XM_011521552.1:c.-3-4369A>C XP_011519854.1:n.-3-4369A>C
XM_005254375.3:c.37-4369A>C XP_005254432.1:n.37-4369A>C
NM_203349.4:c.586-4369A>C MANE Select NP_976224.3:n.586-4369A>C