Canonical Allele Identifier: CA41419403
Gene:

Linked Data

dbSNP Id: rs573758139
MyVariant Identifiers: chr2:g.1557821A>G (hg19) chr2:g.1554049A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.1554049A>G , CM000664.2:g.1554049A>G GRCh38
NC_000002.11:g.1557821A>G , CM000664.1:g.1557821A>G GRCh37
NC_000002.10:g.1536828A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011510447.1:c.-1124A>G XP_011508749.1:n.-1124A>G
XM_011510448.1:c.-1124A>G XP_011508750.1:n.-1124A>G
XR_922720.1:n.85+2449T>C
XM_017005455.1:c.-1124A>G XP_016860944.1:n.-1124A>G
NR_168373.1:n.746-121A>G
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