Canonical Allele Identifier: CA617849100
Gene: SHC4 HGNC NCBI

Linked Data

dbSNP Id: rs1436398234
gnomAD v2: 15-49221547-T-C
gnomAD v3: 15-48929350-T-C
gnomAD v4: 15-48929350-T-C
MyVariant Identifiers: chr15:g.49221547T>C (hg19) chr15:g.48929350T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48929350T>C , CM000677.2:g.48929350T>C GRCh38
NC_000015.9:g.49221547T>C , CM000677.1:g.49221547T>C GRCh37
NC_000015.8:g.47008839T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000332408.9:c.586-4401A>G MANE Select ENSP00000329668.4:n.586-4401A>G
ENST00000332408.8:c.586-4401A>G ENSP00000329668.4:n.586-4401A>G
NM_203349.3:c.586-4401A>G NP_976224.3:n.586-4401A>G
XM_005254375.2:c.37-4401A>G XP_005254432.1:n.37-4401A>G
XM_011521552.1:c.-3-4401A>G XP_011519854.1:n.-3-4401A>G
XM_005254375.3:c.37-4401A>G XP_005254432.1:n.37-4401A>G
NM_203349.4:c.586-4401A>G MANE Select NP_976224.3:n.586-4401A>G
Search 100 bp 5'
Search 100 bp 3'