Canonical Allele Identifier: CA713423436
Gene: SHC4 HGNC NCBI

Linked Data

dbSNP Id: rs1361672826
MyVariant Identifiers: chr15:g.49221509A>G (hg19) chr15:g.48929312A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48929312A>G , CM000677.2:g.48929312A>G GRCh38
NC_000015.9:g.49221509A>G , CM000677.1:g.49221509A>G GRCh37
NC_000015.8:g.47008801A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000332408.9:c.586-4363T>C MANE Select ENSP00000329668.4:n.586-4363T>C
ENST00000332408.8:c.586-4363T>C ENSP00000329668.4:n.586-4363T>C
NM_203349.3:c.586-4363T>C NP_976224.3:n.586-4363T>C
XM_005254375.2:c.37-4363T>C XP_005254432.1:n.37-4363T>C
XM_011521552.1:c.-3-4363T>C XP_011519854.1:n.-3-4363T>C
XM_005254375.3:c.37-4363T>C XP_005254432.1:n.37-4363T>C
NM_203349.4:c.586-4363T>C MANE Select NP_976224.3:n.586-4363T>C
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