Canonical Allele Identifier: CA2175727375
Gene: SHC4 HGNC NCBI

Linked Data

dbSNP Id: rs1900911267
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48929342G>A , CM000677.2:g.48929342G>A GRCh38
NC_000015.9:g.49221539G>A , CM000677.1:g.49221539G>A GRCh37
NC_000015.8:g.47008831G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000332408.9:c.586-4393C>T MANE Select ENSP00000329668.4:n.586-4393C>T
ENST00000332408.8:c.586-4393C>T ENSP00000329668.4:n.586-4393C>T
NM_203349.3:c.586-4393C>T NP_976224.3:n.586-4393C>T
XM_005254375.2:c.37-4393C>T XP_005254432.1:n.37-4393C>T
XM_011521552.1:c.-3-4393C>T XP_011519854.1:n.-3-4393C>T
XM_005254375.3:c.37-4393C>T XP_005254432.1:n.37-4393C>T
NM_203349.4:c.586-4393C>T MANE Select NP_976224.3:n.586-4393C>T
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