Canonical Allele Identifier: CA107971406
Gene:

Linked Data

dbSNP Id: rs188708470
MyVariant Identifiers: chr4:g.149570730G>A (hg19) chr4:g.148649578G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.148649578G>A , CM000666.2:g.148649578G>A GRCh38
NC_000004.11:g.149570730G>A , CM000666.1:g.149570730G>A GRCh37
NC_000004.10:g.149790180G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939336.1:n.437-30710C>T
XR_001741441.1:n.1745+104994G>A
XR_939336.3:n.2921-30710C>T
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