Canonical Allele Identifier: CA130184675
Gene: ADAM19 HGNC NCBI

Linked Data

dbSNP Id: rs7733662
gnomAD v2: 5-156942240-C-T
gnomAD v3: 5-157515232-C-T
gnomAD v4: 5-157515232-C-T
MyVariant Identifiers: chr5:g.156942240C>T (hg19) chr5:g.157515232C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.157515232C>T , CM000667.2:g.157515232C>T GRCh38
NC_000005.9:g.156942240C>T , CM000667.1:g.156942240C>T GRCh37
NC_000005.8:g.156874818C>T NCBI36
NG_046960.1:g.65592G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000257527.9:c.667-1727G>A MANE Select ENSP00000257527.5:n.667-1727G>A
ENST00000257527.8:c.667-1727G>A ENSP00000257527.4:n.667-1727G>A
ENST00000517905.1:c.667-1727G>A ENSP00000428654.1:n.667-1727G>A
ENST00000517951.5:c.667-1727G>A ENSP00000428376.1:n.667-1727G>A
NM_033274.4:c.667-1727G>A NP_150377.1:n.667-1727G>A
XM_005266003.2:c.667-1727G>A XP_005266060.1:n.667-1727G>A
XM_011534680.1:c.-135-1727G>A XP_011532982.1:n.-135-1727G>A
XM_011534681.1:c.-145-1727G>A XP_011532983.1:n.-145-1727G>A
NM_033274.5:c.667-1727G>A MANE Select NP_150377.1:n.667-1727G>A
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