Canonical Allele Identifier: CA10866266
Gene: FYB2 HGNC NCBI

Linked Data

dbSNP Id: rs6662617
gnomAD v2: 1-57269521-A-G
gnomAD v3: 1-56803848-A-G
gnomAD v4: 1-56803848-A-G
MyVariant Identifiers: chr1:g.57269521A>G (hg19) chr1:g.56803848A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.56803848A>G , CM000663.2:g.56803848A>G GRCh38
NC_000001.10:g.57269521A>G , CM000663.1:g.57269521A>G GRCh37
NC_000001.9:g.57042109A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000343433.7:c.10-11045T>C MANE Select ENSP00000345972.6:n.10-11045T>C
ENST00000343433.6:c.10-11045T>C ENSP00000345972.6:n.10-11045T>C
ENST00000484327.1:n.416-11045T>C
NM_001004303.4:c.10-11045T>C NP_001004303.3:n.10-11045T>C
XM_005270584.3:c.10-11045T>C XP_005270641.1:n.10-11045T>C
XM_011540898.1:c.10-11045T>C XP_011539200.1:n.10-11045T>C
XM_011540899.1:c.10-11045T>C XP_011539201.1:n.10-11045T>C
XM_011540900.1:c.10-11045T>C XP_011539202.1:n.10-11045T>C
XM_011540901.1:c.10-11045T>C XP_011539203.1:n.10-11045T>C
XM_011540902.1:c.10-11045T>C XP_011539204.1:n.10-11045T>C
XM_011540903.1:c.10-11045T>C XP_011539205.1:n.10-11045T>C
XM_011540905.1:c.10-11045T>C XP_011539207.1:n.10-11045T>C
XM_011540907.1:c.10-11045T>C XP_011539209.1:n.10-11045T>C
XR_946569.1:n.416-11045T>C
XR_946570.1:n.416-11045T>C
XR_946571.1:n.416-11045T>C
XR_946572.1:n.416-11045T>C
XM_011540900.2:c.10-11045T>C XP_011539202.1:n.10-11045T>C
XM_011540903.2:c.10-11045T>C XP_011539205.1:n.10-11045T>C
XM_011540905.2:c.10-11045T>C XP_011539207.1:n.10-11045T>C
XM_017000544.2:c.-381-11045T>C XP_016856033.1:n.-381-11045T>C
XM_017000545.1:c.-381-11045T>C XP_016856034.1:n.-381-11045T>C
XM_017000548.1:c.10-11045T>C XP_016856037.1:n.10-11045T>C
XM_024453853.1:c.10-11045T>C XP_024309621.1:n.10-11045T>C
XR_001737026.1:n.416-11045T>C
XR_946572.2:n.416-11045T>C
NM_001004303.5:c.10-11045T>C MANE Select NP_001004303.3:n.10-11045T>C
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