Canonical Allele Identifier: CA99707000

Gene: ALB

Linked Data

• dbSNP Id: rs966868402
• gnomAD v4: 4-73414940-G-C
• MyVariant Identifiers: chr4:g.74280657G>C (hg19) ; chr4:g.73414940G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73414940G>C , CM000666.2:g.73414940G>C	GRCh38
NC_000004.11:g.74280657G>C , CM000666.1:g.74280657G>C	GRCh37
NC_000004.10:g.74499521G>C	NCBI36
NG_009291.1:g.15686G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1059-95G>C MANE Select	ENSP00000295897.4:n.1059-95G>C
ENST00000295897.8:c.1059-95G>C	ENSP00000295897.4:n.1059-95G>C
ENST00000401494.7:c.714-95G>C	ENSP00000384695.3:n.714-95G>C
ENST00000415165.6:c.483-95G>C	ENSP00000401820.2:n.483-95G>C
ENST00000476441.6:c.*338-95G>C	ENSP00000423727.1:n.*338-95G>C
ENST00000484992.1:n.379-95G>C
ENST00000503124.5:c.609-95G>C	ENSP00000421027.1:n.609-95G>C
ENST00000504043.1:n.62-95G>C
ENST00000505649.5:n.745-95G>C
ENST00000509063.5:c.1059-95G>C	ENSP00000422784.1:n.1059-95G>C
ENST00000511370.1:c.592-95G>C
ENST00000621085.4:c.491-166G>C	ENSP00000483421.1:n.491-166G>C
ENST00000621628.4:c.487-162G>C	ENSP00000480485.1:n.487-162G>C
NM_000477.5:c.1059-95G>C	NP_000468.1:n.1059-95G>C
NM_000477.6:c.1059-95G>C	NP_000468.1:n.1059-95G>C
NM_000477.7:c.1059-95G>C MANE Select	NP_000468.1:n.1059-95G>C