Canonical Allele Identifier: CA155844876
Gene:

Linked Data

dbSNP Id: rs543446104
MyVariant Identifiers: chr7:g.24452929A>G (hg19) chr7:g.24413310A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.24413310A>G , CM000669.2:g.24413310A>G GRCh38
NC_000007.13:g.24452929A>G , CM000669.1:g.24452929A>G GRCh37
NC_000007.12:g.24419454A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017012910.1:c.-89+31749T>C XP_016868399.1:n.-89+31749T>C
XM_017012911.1:c.-89+31749T>C XP_016868400.1:n.-89+31749T>C
XR_001745121.1:n.344+31749T>C
XR_001745122.1:n.344+31749T>C
XR_001745123.1:n.344+31749T>C
XR_001745124.1:n.344+31749T>C
XR_001745125.1:n.344+31749T>C
XR_001745126.1:n.344+31749T>C
XR_001745127.1:n.344+31749T>C
XR_001745129.1:n.344+31749T>C
XR_001745130.1:n.344+31749T>C
XR_001745131.1:n.344+31749T>C
XR_001745132.1:n.344+31749T>C
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