Canonical Allele Identifier: CA269565204
Gene: SHC4 HGNC NCBI

Linked Data

dbSNP Id: rs561398218
gnomAD v2: 15-49221540-G-C
gnomAD v3: 15-48929343-G-C
gnomAD v4: 15-48929343-G-C
MyVariant Identifiers: chr15:g.49221540G>C (hg19) chr15:g.48929343G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48929343G>C , CM000677.2:g.48929343G>C GRCh38
NC_000015.9:g.49221540G>C , CM000677.1:g.49221540G>C GRCh37
NC_000015.8:g.47008832G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000332408.9:c.586-4394C>G MANE Select ENSP00000329668.4:n.586-4394C>G
ENST00000332408.8:c.586-4394C>G ENSP00000329668.4:n.586-4394C>G
NM_203349.3:c.586-4394C>G NP_976224.3:n.586-4394C>G
XM_005254375.2:c.37-4394C>G XP_005254432.1:n.37-4394C>G
XM_011521552.1:c.-3-4394C>G XP_011519854.1:n.-3-4394C>G
XM_005254375.3:c.37-4394C>G XP_005254432.1:n.37-4394C>G
NM_203349.4:c.586-4394C>G MANE Select NP_976224.3:n.586-4394C>G
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