Canonical Allele Identifier: CA784579208
Gene:

Linked Data

dbSNP Id: rs1380827711
MyVariant Identifiers: chr4:g.103421133T>C (hg19) chr4:g.102499976T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102499976T>C , CM000666.2:g.102499976T>C GRCh38
NC_000004.11:g.103421133T>C , CM000666.1:g.103421133T>C GRCh37
NC_000004.10:g.103640165T>C NCBI36
NG_050628.1:g.3648T>C

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.643+1273A>G XP_011530769.1:n.643+1273A>G
NR_136202.1:n.48+2463A>G
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