Canonical Allele Identifier: CA103120435
Gene:

Linked Data

dbSNP Id: rs748338482
MyVariant Identifiers: chr4:g.103422173G>C (hg19) chr4:g.102501016G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102501016G>C , CM000666.2:g.102501016G>C GRCh38
NC_000004.11:g.103422173G>C , CM000666.1:g.103422173G>C GRCh37
NC_000004.10:g.103641205G>C NCBI36
NG_050628.1:g.4688G>C

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.643+233C>G XP_011530769.1:n.643+233C>G
NR_136202.1:n.48+1423C>G
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