Canonical Allele Identifier: CA735541215
Gene:

Linked Data

dbSNP Id: rs1435511784
gnomAD v3: 1-38158441-A-G
gnomAD v4: 1-38158441-A-G
MyVariant Identifiers: chr1:g.38624113A>G (hg19) chr1:g.38158441A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.38158441A>G , CM000663.2:g.38158441A>G GRCh38
NC_000001.10:g.38624113A>G , CM000663.1:g.38624113A>G GRCh37
NC_000001.9:g.38396700A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_947202.1:n.45-3252A>G
XR_947203.1:n.61+16727A>G
XR_947204.1:n.45-3252A>G
XR_947205.1:n.45-3252A>G
XR_001737984.1:n.45-3252A>G
XR_001737985.1:n.61+16727A>G
XR_001737986.1:n.45-3252A>G
XR_001737987.1:n.45-3252A>G
XR_002958294.1:n.45-3252A>G
XR_947205.2:n.45-3252A>G
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