Canonical Allele Identifier: CA1880524664
Gene:

Linked Data

dbSNP Id: rs1841645162
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.128945516A>G , CM000671.2:g.128945516A>G GRCh38
NC_000009.11:g.131707795A>G , CM000671.1:g.131707795A>G GRCh37
NC_000009.10:g.130747616A>G NCBI36
NG_017009.1:g.7218T>C , LRG_744:g.7218T>C
NG_033111.1:g.2824A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000482796.1:c.39-3673A>G ENSP00000417556.2:n.39-3673A>G
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