Canonical Allele Identifier: CA130182498
Gene: ADAM19 HGNC NCBI

Linked Data

dbSNP Id: rs999025981
gnomAD v2: 5-156970168-T-G
gnomAD v3: 5-157543160-T-G
gnomAD v4: 5-157543160-T-G
MyVariant Identifiers: chr5:g.156970168T>G (hg19) chr5:g.157543160T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.157543160T>G , CM000667.2:g.157543160T>G GRCh38
NC_000005.9:g.156970168T>G , CM000667.1:g.156970168T>G GRCh37
NC_000005.8:g.156902746T>G NCBI36
NG_046960.1:g.37664A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000257527.9:c.252-5169A>C MANE Select ENSP00000257527.5:n.252-5169A>C
ENST00000257527.8:c.252-5169A>C ENSP00000257527.4:n.252-5169A>C
ENST00000517905.1:c.252-5169A>C ENSP00000428654.1:n.252-5169A>C
ENST00000517951.5:c.252-5169A>C ENSP00000428376.1:n.252-5169A>C
NM_033274.4:c.252-5169A>C NP_150377.1:n.252-5169A>C
XM_005266003.2:c.252-5169A>C XP_005266060.1:n.252-5169A>C
NM_033274.5:c.252-5169A>C MANE Select NP_150377.1:n.252-5169A>C
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