Canonical Allele Identifier: CA269565232
Gene: SHC4 HGNC NCBI

Linked Data

dbSNP Id: rs1030043054
gnomAD v2: 15-49221557-A-G
MyVariant Identifiers: chr15:g.49221557A>G (hg19) chr15:g.48929360A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48929360A>G , CM000677.2:g.48929360A>G GRCh38
NC_000015.9:g.49221557A>G , CM000677.1:g.49221557A>G GRCh37
NC_000015.8:g.47008849A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000332408.9:c.586-4411T>C MANE Select ENSP00000329668.4:n.586-4411T>C
ENST00000332408.8:c.586-4411T>C ENSP00000329668.4:n.586-4411T>C
NM_203349.3:c.586-4411T>C NP_976224.3:n.586-4411T>C
XM_005254375.2:c.37-4411T>C XP_005254432.1:n.37-4411T>C
XM_011521552.1:c.-3-4411T>C XP_011519854.1:n.-3-4411T>C
XM_005254375.3:c.37-4411T>C XP_005254432.1:n.37-4411T>C
NM_203349.4:c.586-4411T>C MANE Select NP_976224.3:n.586-4411T>C
Search 100 bp 5'
Search 100 bp 3'